ATCC - Animal Cell Culture Guide PDF

ATCC ANIMAL CELL CULTURE GUIDE
tips and techniques for continuous cell lines
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Table of Contents
This guide contains general technical information for working with animal cells in culture, including media,
subculturing, cryopreservation and contamination. A more comprehensive reference on animal cell culture
can be found in Culture of Animal Cells: A Manual of Basic Technique, 5th edition, by R. Ian Freshney (24).
Getting Started with an ATCC Cell Line.............1 Culture Vessels and Surfaces................................... 20
Product Sheet..............................................................1 Vessels......................................................................... 20
Preparation of Medium............................................1 Surface Coatings and Feeder Cells.................... 22
Initiating Frozen Cultures........................................1
Processing Flask Cultures........................................1 Cryopreservation............................................................... 24
Overview.................................................................... 24
Cell Growth and Propagation....................................4 Freeze Medium........................................................ 24
Passage Number and Population Doubling Equipment................................................................. 25
Level................................................................................4 Liquid Nitrogen Freezer Storage....................... 26
Adapting to a New Medium or Serum...............5 Cryopreservation Procedure............................... 26
Temperature.................................................................5 Recovery of Cryopreserved Cells....................... 27
Examination of Cultures..........................................6
Cell Counting...............................................................6 Contamination and Biosafety................................. 28
Cell Viability..................................................................7 Check for Microbial Contamination................. 28
Subculturing Monolayer Cells...............................8 Mycoplasma Contamination............................... 28
Monolayer Subculturing..........................................8 Treating for Microbiobial Contamination....... 29
Troubleshooting Monolayer Cell Subculturing...9 Cellular Cross-Contamination............................. 29
Suspension Cells...................................................... 10 Biosafety..................................................................... 30
Suspension Cell Subculturing............................. 10
Troubleshooting Suspension Cell Subculturing... 11 Glossary...................................................................................... 31
Adapting a Monolayer Cell Line to Grow in
Suspension................................................................ 11 References................................................................................ 34
Complete Growth Media............................................. 13 ATCC Media, Sera, and Reagents......................... 35

Cell Culture Media................................................... 13
Media Formulations............................................... 14
Media Ingredients................................................... 14
Media Supplements............................................... 16
Osmolality.................................................................. 17
Antibiotics and Antimycotics.............................. 17
Animal Sera............................................................... 18
Phone 800.638.6597 www.atcc.org

Getting Started with an ATCC Cell Line
ATCC cell lines and hybridomas are shipped frozen on dry ice in cryopreservation vials or as growing
cultures in flasks at ambient temperature. Upon receipt of frozen cells, it is important to immediately revive
them by thawing and removing the DMSO and placing them into culture. If this is not possible, store the
cells in liquid nitrogen vapor (below 130C). Do not store frozen cells at temperatures above 130C as
their viability will decline rapidly.
Product Sheet
ATCC cell lines come with a Product Sheet that contains detailed information for handling the cells. An
abbreviated version may be found at the ATCC website or call ATCC Technical Service Department to
request a copy. The Product Sheet also contains batch-specific information such as the number of cells per
vial, the recommended split or subcultivation ratio, and the passage number when known.
Preparation of Medium
Prepare for reviving cell lines by assembling the appropriate medium,
NOTE 1:
serum, and additional reagents required for growth. Many of these products While most cell lines can replicate
are available from ATCC and can be ordered with the cell lines. These are in more than one culture medium,
the same reagents used by ATCC for cell growth and preservation. (See: their characteristics may alter when
the medium is changed. For this
NOTE 1) reason, starting cell cultures in
the same medium used by ATCC is
Initiating Frozen Cultures recommended for the best results
(see the Product Information Sheet
and ATCC website). For details
1. Prepare a culture vessel so that it contains the recommended volume on adapting a cell line to a new
of the appropriate culture medium as listed on the Product Sheet, medium, see page 5.
equilibrated for temperature and pH (CO).
2. Thaw the vial by gentle agitation in a water bath at 37C or the normal growth temperature for that cell
line. Thawing should be rapid, approximately 2 minutes or until ice crystals have melted.
3. Remove the vial from the water bath and decontaminate it by dipping in or spraying with 70% ethanol.
Follow strict aseptic conditions in a laminar flow tissue culture hood for all further manipulations.
4. Unscrew the top of the vial and transfer the contents to a sterile
NOTE 2:
centrifuge tube containing 9 mL of the recommended medium. Some cell lines, such as hybridomas,
Remove the cryoprotectant agent (DMSO) by gentle centrifugation (10 take several days before fully
minutes at 125 g). Discard the supernatant, and resuspend the cells recovering from cryopreservation.
in 1 or 2 mL of complete growth medium. Transfer the cell suspension Some hybridomas have poor
viability the first day in culture
into the culture vessel containing the complete growth medium and and will generate cellular debris.
mix thoroughly by gentle rocking. After this point, the cells will begin
to recover and enter exponential
5. Examine the cell cultures after 24 hours and subculture as needed. growth.
(See: NOTE 2)
Processing Flask Cultures

Some ATCC cell, are shipped as growing cultures in culture vessels. These vessels are seeded with cells,
incubated to ensure cell growth and then filled completely with medium for shipping.
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Upon receiving a flask culture, visually examine the medium for
macroscopic evidence of microbial contamination. This includes
unusual pH shifts (yellow or purple color from the phenol red),
turbidity, or particles. With an inverted microscope at low power
(100) check the medium for evidence of microbial contamination
as well as the morphology of the cells. See page 6 for more details
on examining cell cultures.
If the cells are attached and growing in a monolayer:
1. Aseptically remove all but 5 mL to 10 mL of the shipping
medium. The shipping medium can be saved for reuse and
should be stored at 4C.
2. Incubate the flask at the temperature and CO concentration recommended on the Product Sheet
(37C with 5% CO for most cell lines) until the cells are subcultured.
If the cells are not attached or are growing in suspension:
1. Aseptically transfer the entire contents of the flask to a centrifuge tube.
2. Centrifuge at 125 g for 5 to 10 minutes.
3. Remove all but 10 mL of the shipping medium supernatant and resuspend the cells. Store the remainder
of this medium at 4C for later use.
4. Aseptically transfer the resuspended cells to a 25-cm flask or 75-cm flask, depending upon the cell
line (see the Product Sheet).
5. Incubate the cells at the temperature and CO concentration recommended on the Product Information
Sheet until cells are subcultured.
Most cell lines begin as primary cultures originating from a piece of minced or enzyme-dispersed tissue.
Primary cultures, as mixtures of several cell types, retain the characteristics of their source tissue.
After a period of time, primary cultures will reach confluency, the state when all available space of the
culture vessel is covered due to cellular expansion. At this point, the culture will need to be disaggregated
(usually with proteolytic enzymes like trypsin) into individual cells and subcultured (split, passaged,
or transferred). Following this first passage, the culture is generally referred to as a cell line. With each
subsequent subculture, the cellular population becomes more homogeneous as the faster growing cells
predominate. Cells with desired properties can also be selected out of the culture by cloning.
Diploid cell lines rarely progress beyond a few population doublings. They have a finite replicative capacity
and begin to slow down and eventually stop dividing after 20 to 80 population doublings. Recent evidence
suggests that some of the observed cellular senescence in cell culture may be due to inappropriate culture
conditions as opposed to a predetermined replicative senescence. Still other data support replicative
senescence for the cells of some species (notably human) even when grown in improved culture conditions.
This senescence is mediated by the shortening of the ends of the chromosomes (telomeres) with each cell
division.
In contrast, continuous (or immortalized) cell lines have infinite replicative capacity. These lines are
derived from cell lines through immortalization or transformation by any one of a number of means.
Many continuous cell lines were derived from tumor tissue. Most of the cell lines in the ATCC collection
are continuous, though a few, such as CCD-1117Sk human skin fibroblast (ATCC CRL-2465) or CCD-18Co
human colon (ATCC CRL-1459) are finite. For more information about ATCC immortalized cell lines see
the website.
Phone 800.638.6597 www.atcc.org page 2

As noted in the section on culture vessels, cell lines grow either attached to a surface (anchorage dependent)
or in suspension (anchorage independent). As cells grow and divide in a monolayer or in suspension, they
usually follow a characteristic growth pattern composed of four phases: Lag, log or exponential, stationary
or plateau and decline.
Lag phase Immediately after seeding of the culture vessel, the cells grow slowly while recovering
from the stress of sub-culturing.
Log or exponential phase The cells enter a period of exponential growth that lasts until the entire
growth surface is occupied or the cell concentration exceeds the capacity of the medium.
Stationary phase Cell proliferation slows and stops.
Decline phase If the culture medium is not replaced and the cell number is not reduced, the cells
lose viability and their number decreases.
To ensure viability, genetic stability, and phenotypic stability, cell lines need to be maintained in the
exponential phase. This means that they need to be subcultured on a regular basis before they enter the
stationary growth phase, before a monolayer becomes 100% confluent or before a suspension reaches its
maximum recommended cell density. Generating a growth curve for each cell line is useful to determine
the growth characteristics of the cell line. (See: Figure 1)
For detailed information on the growth and propagation of any ATCC cell line, see the specific cell line
Product Sheet which is included with every shipment. An abbreviated version may also be found on the
ATCC website, or call ATCC Technical Service to have one sent to you.

Cell Growth and Propagation
Passage Number and Population Doubling Level
Primary cultures are generally subcultured at a 1:2 ratio (they are split in half with each passage). Most
continuous cell lines replicate at higher rates and are subcultured at a much higher split ratio. Passage
number is generally the number of times the cells have been subcultured into a new vessel. For diploid
cultures, passage number is roughly equal to the number of population doublings (or population doubling
level, PDL) since the culture was started. This is not the case for continuous cell lines as they are passaged at
higher split ratios. Consequently the PDL is not determined for continuous cell lines. In most cases, the PDL
is an estimate as it does not account for any cells that were lost due to death from necrosis or apoptosis or
cells which are nearing senescence and no longer divide. Calculate the population doubling level with the
following formula:
PDL = 3.32 (log Xe log Xb) + S
Xb is the cell number at the beginning of the incubation time.
Xe is the cell number at the end of the incubation time.
S is the starting PDL.
Lag Phase Exponential Phase Stationary Phase

3 x 105
Subculture
105
Cells/cm2
104
Doubling Time
3 x 103
0 1 2 3 4 5 6 7 8 9 10
Days After Subculture
Figure 1. Growth curve for cells grown in culture. Cells should be subcultured while
still in the exponential phase.
Calculate the population doubling time, or the time required for a culture NOTE:
to double in number, with the following formula: Cells grow at different rates in
each of the different phases of the
DT=T ln2/ln(Xe/Xb) growth cycle and the calculated
doubling time may be a composite
T is the incubation time in any units. of growth during more than one
Xb is the cell number at the beginning of the incubation time. of these phases. Growth during
exponential growth or log phase
Xe is the cell number at the end of the incubation time. is fairly constant and reproducible
(See: NOTE) for a given set of growth conditions.

ATCC tracks the PDL and passage number for many adherent cell lines when the depositor supplies this
information at the time of deposit. See the Product Information Sheet for the specific cell line for the
passage number and/or PDL as part of the batch-specific information supplied.
Adapting to a New Medium or Serum

To ensure that the characteristics of your cell line remain constant, maintain your cells in the same medium,
serum, and supplements with the same subculturing regimen used to establish the culture. Any change to
the culturing conditions has the potential to change the characteristics of the cell line.
Be particularly cautious when working with a new cell line as media formulations vary among suppliers, even
for media with similar or identical names. Read descriptions, formulations, and labels carefully to ensure
that the appropriate medium is used or the cell line may be inadvertently adapted to a new medium. All
ATCC cell lines come with information on their growth medium. In most cases, the recommended medium
and serum can be purchased from ATCC along with the cell line.
Use the following procedure to adapt a cell line to a new medium:
1. Subculture the line at a 1:2 split ratio (split the culture in half ) into two vessels.
Maintain one with the original medium and continue to subculture these cells for the entire adaptation
process. Use a 1:1 mix of the original and new medium in the second vessel. The culture grown in the
original medium serves as a reference point as well as a safeguard in case the adapting cells do not
survive the process. The low split ratio helps mitigate the stress associated with subculturing as well as
with the new medium.
2. Monitor cell growth in the two media and watch for any change in morphology or growth rate. If they
are identical, subculture the adapting cells at the next passage with a 1:2 split ratio in a 1:3 medium mix
(25% original, 75% new).
3. Monitor the growth rate and morphology of the original and adapting cultures.
At the next passage, split the adapting cultures 1:2 in a 1:7 medium mix (12.5% original, 87.5% new).
4. Monitor the growth rate and morphology of the original and adapting cultures. If the cells are identical,
then at the next passage split the adapting cells 1:2 in 100% new medium. At this point, the culture
should be adapted to the new medium.
To confirm complete adaptation to the new medium, perform functional tests on cells derived from the
original and new medium. If at any point in the process the adapting culture fails to perform as well as
the reference culture, then allow the adapting culture more time and a few more passages in their current
medium mix (e.g., 1:3, 1:7, etc.) until they match the reference cells.
The same approach can be used to adapt cells to serum-free medium; simply decrease the serum level in
the medium by half with each passage until a 0.06% (or lower) serum level is reached. At this point, the cells
can be maintained in serum-free medium. If at any point the growth rate declines, then the serum level
should be increased to the level where the cells grew normally. In this procedure, start with the serum-free
medium supplemented with serum so that only the level of serum changes with each passage.
Temperature NOTE:
Regularly calibrate the temperature
Most animal cell lines require 37C for optimum growth. Insect and control system of incubators and
use an alarm system when possible
amphibian cells require lower temperatures (such as 28C) as do some to warn against temperature
animal cell lines which are temperature sensitive for their phenotypic increases above the optimum
characteristics. While cultured cells can withstand considerable drops in setting.

temperature and most can survive for several days at 4C, few can tolerate even a few hours at more than
2C above their optimal temperature. (See: NOTE)
Examination of Cultures
Observe the morphology and viability of cultures regularly and carefully. Examine the medium in the vessel
for macroscopic evidence of microbial contamination. This includes unusual pH shifts (yellow or purple
color from the phenol red), turbidity, or particles. Also, look for small fungal colonies that float at the
medium-air interface. Specifically check around the edges of the vessel as these may not be readily visible
through the microscope.
With an inverted microscope at low power (40), check the medium for evidence of microbial contamination
and the morphology of the cells. Bacterial contamination will appear as small, shimmering black dots
within the spaces between the cells. Yeast contamination will appear as rounded or budding particles,
while fungi will have thin filamentous mycelia. For nonadherent cells grown in flasks, such as hybridomas,
this is a simple matter of viewing the flask directly on the microscope. For cells grown in spinner flasks or
bioreactors, a sample of the cell suspension will need to be withdrawn and loaded into a microscope slide
or hemocytometer for observation.
Most adherent cells should be attached firmly to the surface. In some cases, healthy cells will round up and
detach somewhat during mitosis and appear very refractile. Following mitosis, they will reattach. Some of
these will float free if the culture vessel is physically disturbed. In contrast, dead cells often round up and
detach from the monolayer and appear smaller and darker (not refractile) than healthy cells.
Cells in suspension culture grow either as single cells or as clusters of cells. Viable cells appear round and
refractile whereas dead cells appear smaller and darker. Occasionally, a portion of the cells will attach and
grow on the side of the culture vessel and appear round or flattened. The percentage of attached cells
varies with the culture conditions and the cell density. Cellular debris may also be observed in healthy cell
populations. Some cell lines grow as mixed adherent and suspension cultures.
As a reference, photomicrographs for some ATCC cell lines are available on the website. Cells are shown
at two different densities: just after subculturing (low) and just before they need to be subcultured (high).
In addition to daily examinations,
periodically test a sample of
the culture for the presence of
fungi, bacteria, and mycoplasma.
There are several methods that
can be used to check for these
contaminants. For additional
information, refer to the section on
microbial contamination (page 28). ATCC CCL-61 at high density ATCC CCL-61 at low density
Cell Counting
Cell counts are necessary in order to establish or monitor growth rates as well as to set up new cultures
with known cell numbers. Hemocytometers (also spelled hemacytometers) are commonly used to estimate
cell number and determine cell viability. A hemocytometer is a fairly thick glass slide with two counting
chambers, one on each side. Each counting chamber has a mirrored surface with a 3 3 mm grid of 9
counting squares. (See Figure 2) The chambers have raised sides that will hold a coverslip exactly 0.1 mm
above the chamber floor. Each of the 9 counting squares holds a volume of 0.0001 mL.

Hemocytometers are excellent for determining cell viability, but are not precise for determining cell number
due to the relatively low number of cells actually counted. An automated counter will generate the most
reliable data, particularly when used in combination with the viability data from a hemocytometer.
Count cells as follows:
1. Clean, thoroughly dry, and assemble the
1 2 hemocytometer with the cover slip.

2. Transfer a small amount of cell suspension to the edge
of each of the two counting chambers. Allow the cell
suspension to be drawn into the counting chamber
by capillary action.
3. Place the hemocytometer under an inverted
microscope and view the cells at 100 magnification.
4. Focus on the quadrants, labeled 1, 2, 3, and 4 in Figure 2.
5. Record the number of cells in each section. Average
3 4 the number of cells, and multiply by the dilution
factor. If the cells have not been diluted, this factor
will be 10 cells/mL. Any dilution of the sample after it
was removed from the cell suspension, such as using
Figure 2. Hemocytometer grid with Neubauer ruling. vital stain, needs to be included in the calculation.
For example, if the four counts are 60, 66, 69, and 75, the concentration would be 68 10 cells/mL for
the sample that was loaded into the hemocytometer. For best results, adjust the concentration of the
suspension so that 50 to 100 cells are in each of the four sections.
Most cultures will grow at an initial inoculum cell concentration ranging from 10 to 10 cells/cm. Faster-
growing cultures are usually set up at lower concentrations. Some cultures do not grow well unless a
minimum concentration of cells is initially added; see the Product Sheet for details.
Cell Viability
Viability assays measure the number of viable cells in a population. When combined with the total number
of cells, the number of viable cells provides an accurate indication of the health of the cell culture. The most
common and rapid methods rely upon the integrity of the cell membrane as an indicator of cell viability.
Both trypan blue and erythrosin B (ATCC No. 30-2504) stains are actively excluded by viable cells but are
taken up and retained by dead cells, which lack an intact membrane.
While both stains are used in the same way, ATCC recommends erythrosin B in place of trypan blue for
hematopoetic cells. When using trypan blue, incubate cells for two to five minutes prior to use. If not
counted within this time, the cells will begin to deteriorate and take up the dye. Erythrosin B does not
require an incubation period.
Erythrosin B stain generates more accurate results with fewer false negatives and false positives. Erythrosin
B stain solution provides a clear background and does not bind serum proteins as avidly as trypan blue,
making stained cells more distinct and easier to identify. Also, microbial contamination or precipitates in
the cell culture are more readily apparent. Finally, trypan blue is toxic and a potential carcinogen.
For either stain use the following directions:
1. Mix the cell suspension 1:1 with a 0.1% erythrosin B solution in PBS or 0.4% trypan blue solution in PBS.

2. Load the cells in the erythrosin B solution directly into a clean, dry hemocytometer, but incubate the
trypan blue solution for two to five minutes before loading.
3. Nonviable cells will be stained red (erythrosin B) or dark blue (trypan blue). Cell viability is calculated
as the number of unstained or viable cells divided by the total number of cells and expressed as a
percentage.
Subculturing Monolayer Cells

Anchorage-dependent cell lines growing in monolayers need to be subcultured at regular intervals to
maintain them in exponential growth. When the cells are near the end of exponential growth (roughly 70%
to 90% confluent), they are ready to be subcultured. The subculturing procedure, including recommended
split-ratios and medium replenishment (feeding) schedules, for each ATCC cell line is provided on the
Product Information Sheet.
Subcultivation of monolayers involves the breakage of both intercellular and intracellular cell-to-surface
bonds. For some cells that are loosely attached, a sharp blow with the palm of your hand against the side of
the flask can dislodge them. Many require the digestion of their protein attachment bonds with proteolytic
enzymes such as trypsin/EDTA. For some cell lines mechanical forces such as scraping to dislodge the cells is
preferred. After the cells have been dissociated and dispersed into a single-cell suspension, they are diluted
to the appropriate concentration and transferred into fresh culture vessels with the appropriate growth
medium where they will reattach, grow and divide.
The procedure below is appropriate for most adherent cell lines. However, since every cell line is unique,
incubation times and temperature, number of washes or the solution formulations may vary. In all cases,
continually observe the cells with a microscope during the dissociation process to prevent damage by
the dissociation solution. The amounts used in this procedure are for a 75-cm flask. Adjust volumes as
appropriate for different sized vessels.
Monolayer Subculturing
1. Bring the trypsin-EDTA solution (ATCC No. 30-2101), balanced salt solution [Dulbeccos Phosphate
Buffered Saline without calcium or magnesium, ATCC No. 30-2200], and complete growth medium to
the appropriate temperature for the cell line. In most cases, this is the temperature used to grow the
cells (usually 37C). For some sensitive cells, the trypsin-EDTA solution may need to be used at room
temperature or 4C.
2. Remove and discard the cell culture medium from the flask.
3. Rinse the cell monolayer with Dulbeccos PBS without calcium or magnesium and remove.
4. Add 2 mL to 3 mL of the trypsin-EDTA solution and incubate at the appropriate temperature. Check
the progress of cell dissociation by microscopy. To avoid clumping, do not agitate the cells by hitting or
shaking the flask while waiting for them to detach.
5. Once the cells appear to be detached (5 to 15 minutes for most cell NOTE:
lines; they will appear rounded and refractile under the microscope), For serum-free or low-serum
add 6 to 8 mL of complete growth medium with a pipette to the medium, remove the trypsin-EDTA
cell suspension to inactivate the trypsin. Gently wash any remaining solution by gentle centrifugation
(10 minutes at 125 g) and then
cells from the growth surface of the flask. Check the cells with the resuspend the cells in 6 mL to 8 mL
microscope to be sure that most (>95%) are single cells. If cell clusters of fresh medium. In some cases, the
are apparent, continue to disperse the cells with gentle pipetting. trypsin will need to be inactivated
with a trypsin inhibitor.
(See: NOTE)

6. Add 12 mL to 15 mL of fresh culture medium to a new flask and equilibrate this medium to the
appropriate pH and temperature.
7. Count the cells in suspension and determine their viability or simply divide them according to a routine
split ratio and dispense them into the medium of the newly prepared flask. Do not add a concentrated
cell suspension to an empty culture vessel as this can result in uneven cell attachment and growth.
8. Place the flask back into the incubator. Examine the culture the following day to ensure the cells have
reattached and are actively growing. Change the medium as needed; for most actively growing cultures
two to three times per week is typical.
Troubleshooting Monolayer Cell Subculturing

Cells are difficult to remove.
Inhibitors in the medium (such as serum) have inactivated the dissociating agents. Rinse the cell
monolayer twice with Dulbeccos PBS without calcium or magnesium before adding the dissociating
solution. Or use the trypsin-EDTA solution in place of the Dulbeccos PBS for the first rinse of the
monolayer.
The dissociating solution was too weak. Use higher enzyme concentrations, higher EDTA concentrations,
or different and/or additional enzymes (e.g., dispase, collagenase). Or incubate the cells at 37C to
increase the activity of the dissociating solution.
The cells have been confluent for too long and the cell-to-cell junctions are so tight they prevented the
dissociation agents from reaching the substrate-cell interface. In the future, subculture the cells before
they become confluent.
Cells form clumps after dissociation.
The dissociation procedure was too harsh and genomic DNA was released from lysed cells. Either
the pipetting was too vigorous or the dissociating solution was too strong or too toxic (i.e., the pH
or osmolality of the buffer was incorrect). Add a drop of sterile DNAse (1 mg/mL in water) to the cell
suspension to break down the DNA strands. In the future, treat the cells more gently during pipetting,
shorten the incubation period, use a weaker dissociation solution (lower the enzyme concentration or
remove the EDTA), or incubate at a lower temperature.
The cells aggregated before dilution and dispersion into the medium. Hold the cell suspension on ice if
there will be a delay between removing the cells from the flask growth surface and seeding a new flask.
The cells were centrifuged too hard or too long when removing excess dissociation solution. Be sure to
use gentle centrifugation (10 minutes at 125 g).
Cells have difficulty reattaching to the flask.
The dissociation procedure was too long and stripped away necessary attachment proteins from the
cell membrane.
Insufficient serum or attachment factors were present in the medium (common with serum-free
medium). Add attachment factors to the medium and/or use a protein-coated flask (collagen, poly-L-
lysine, fibronectin, gelatin, etc.).
The dissociating solution was not inactivated or removed by centrifugation. Add additional serum or
specific enzyme inhibitors (e.g., soybean trypsin inhibitor) to the neutralizing medium or centrifuge
(5 minutes at 125 g) the cells down from the dissociation solution and resuspend in fresh medium.

Viability is lower than expected.
The dissociating procedure was too harsh.
The pH or osmolality of the balanced salt solution containing the dissociation agents is incorrect. Check
these directly and/or use a fresh bottle.
The dispersed cell suspension was left too long at too high a cell concentration prior to reseeding. Keep
the cells on ice.
The medium was faulty. Use the recommended formulation and make sure it contains all of the required
additives.
Suspension Cells
Most primary cultures, finite cell lines, and continuous cell lines are anchorage dependent and thus grow
in monolayers attached to a surface. Other cells, particularly those derived from hematopoietic or certain
tumor tissues, are anchorage independent and grow in suspension.
Cell propagation in suspension has several advantages over propagation in monolayer. Subculturing is a
simple matter of dilution. There is little or no growth lag after splitting a suspension culture as there is with
a monolayer culture, because there is none of the trauma associated with proteolytic enzyme dispersal.
Suspension cultures require less lab space per cell yield, and scale-up is straightforward. Cells can be
propagated in bioreactors similar to the fermentors used for yeast or bacteria cultures.
Depending upon the cell type, suspension cultures are seeded at densities from 2 10 to 5 10 viable
cells/mL and can attain densities of 2 10 cell/mL. If cells are seeded at too low a density they will go
through a lag phase of growth, grow very slowly, or die out completely. If cell densities are allowed to
become too high, the cells may exhaust the nutrients in the medium and die abruptly. Recommended
seeding and subculturing densities, media replenishment (feeding) schedules, and medium formulations
for each ATCC cell line are provided on the Product Sheet as well as in the catalog description on the website.
Suspension Cell Subculturing

1. Bring the complete growth medium to the appropriate temperature (usually 37C) in a water bath.
2. Thoroughly mix the cell/medium suspension; use a pipette to suspend cells grown in stationary flasks.
Remove a small amount of the cell suspension to determine the cell density and viability using a
hemocytometer and vital stain (page 7).
3. Calculate the volume of cells required to re-seed the flask at the minimum density for that cell line,
taking into consideration the amount of fresh medium that will be used.
4. Add the appropriate volume of medium to the culture vessel and then add the cell suspension. Do not
add the concentrated cell suspension to an empty flask. The same culture vessel can be reused, but the
chances of contamination increase with each reseeding due to the buildup of small spills of medium
on the flask opening.
5. If necessary, gas the atmosphere of the flask with sterile-filtered CO, seal the flask, and then incubate
at the appropriate temperature.
It is generally not necessary to completely change the medium unless the cells attain a very high density
or the medium has an acidic pH (yellow in color from the phenol red). To completely replace the medium,
centrifuge the cells gently (10 minutes at 125 g), decant the medium, and then resuspend the cells in fresh
medium at the lower seeding density.

Troubleshooting Suspension Cell Subculturing
Viability is lower than expected.
The cell suspension was left too long at too high a cell concentration prior to subculture. In this case,
the medium will have a low pH and be yellow in color. Completely change the medium by gently
centrifuging the cells and resuspend in fresh medium at the lower seeding density.
The cell suspension was diluted below the recommended cell density range. Recover the cells by
centrifugation and resuspend in fresh medium at the appropriate cell density.
The harvesting procedure was too harsh (pipetting too vigorous, cells were centrifuged too hard or too
long, cells damaged during scraping or banging).
The medium was faulty. Use the recommended formulation and make sure it contains all of the required
additives.
Adapting a Monolayer Cell Line to Grow in Suspension

Some cell lines such as L-929 (ATCC CCL-1), HeLa (ATCC CCL-2) and BHK-21 (ATCC CCL-10) can
be adapted to grow in suspension. With time, a population of cells can be selected that does not self-
aggregate or adhere to a growth surface as readily as the parental line. However, the newly selected line
may have lost or acquired characteristics that are different from the original cell population. In most cases
it will be necessary to maintain the culture in suspension with mechanical stirring. Keep in mind that most
anchorage-dependent cells will grow in suspension only with the use of microcarrier beads.
The procedure below was developed for BHK-21 cells, but can be used as a starting point for most cell lines.
1. Dissociate the cell monolayer using standard procedures. Centrifuge and resuspend the cell suspension
in an appropriate spinner medium such as Jokliks modified Eagles Minimum Essential Medium (EMEM).
Spinner media have reduced levels of calcium and magnesium.
2. Count the cell suspension, and then seed two or more spinner flasks with 5 10 cells/mL. This density
may need to be adjusted for your particular cell line. The sides of the culture flask may need to be
siliconized to prevent the cells from sticking to the glass.
3. Observe the cultures daily. Remove samples and record the number of viable cells for each flask.
4. Every three days, collect the cells growing in suspension by centrifugation (10 minutes at 125 g).
Count, and re-seed a fresh flask with fresh medium at 2.5 10 cells/mL. Depending on how well (or
not) the cells adapt to growth in suspension, they may need to be combined with cells from different
flasks to achieve the necessary cell density.
5. If there is a significant amount of cells attached to the walls of the culture vessel, particularly at the
surface of the medium, remove them with trypsin-EDTA and discard them. If the cells in suspension are
badly clumped, they can be dispersed with the trypsin-EDTA solution, collected by centrifugation, and
then re-seeded into the flask as the appropriate density. This treatment may be necessary for the first
few subcultures.
6. Continue to monitor the cells and subculture them every three days. Over time, they should adapt to
growth in suspension and attain a constant growth rate.
A complete growth medium consists of a basal cell culture medium supplemented with ingredients such as
sera, growth factors, trace elements, and hormones. There are numerous formulations ranging from simple,
basic mixtures containing the minimum requirements for growing many cell lines to complex serum-free

mixtures specific for growing a single fastidious cell line. The choice of a NOTE:
medium for a particular cell line is somewhat empirical. Many medium Formulations can vary widely
formulations are available commercially in powder or liquid form. (See: among suppliers, even for media
NOTE) with similar or identical names. Be
sure to read catalog descriptions,
ATCC lists complete medium formulations, plus all handling and passage formulations, and medium labels
carefully to ensure that the
information, for all ATCC cell lines both in the online catalog description appropriate medium is used. For
and on the Product Sheet that accompanies the cell line when shipped. best results start cell cultures in the
Additionally, ATCC offers a full line of media, sera, and reagents for culturing same medium used and distributed
by ATCC (listed on the Product
cells. These are the same reagents used at ATCC for cell growth and Sheet).
propagation. See page 13 for descriptions of ATCC cell culture products.

Complete Growth Media
Cell Culture Media
Cell culture media are complex mixtures of salts, carbohydrates, vitamins, amino acids, metabolic precursors,
growth factors, hormones, and trace elements. The requirements for these components vary among cell
lines, and these differences are partly responsible for the extensive number of medium formulations.
Carbohydrates are supplied primarily in the form of glucose. In some instances, glucose is replaced with
galactose to decrease lactic acid build-up, as galactose is metabolized at a slower rate. Other carbon sources
include amino acids (particularly L-glutamine) and pyruvate.
In addition to nutrients, the medium helps maintain the pH and osmolality in a culture system. The pH is
maintained by one or more buffering systems; CO/sodium bicarbonate, phosphate, and HEPES are the
most common. Sera will also buffer a complete medium. Phenol red, a pH indicator, is added to medium to
colorimetrically monitor changes in pH. Commonly used culture media include the following:
Eagles Minimum Essential Medium (EMEM) was among the first widely used media and was formulated
by Harry Eagle from his earlier and simpler basal medium (BME). BME was developed for culturing mouse
L cells (ATCC CCL-1) and HeLa cells (ATCC CCL-2). Over time, there have been numerous variations on
the EMEM formula for different applications. ATCC EMEM (ATCC No. 30-2003) contains Earles balanced
salt solution, nonessential amino acids, and sodium pyruvate. It is formulated with a reduced sodium
bicarbonate concentration (1,500 mg/l) for use with 5% CO (see Sodium Bicarbonate and Buffering, page 14).
Because EMEM is a simple medium, it is often fortified with additional supplements or higher levels of
serum.
Dulbeccos Modified Eagles Medium (DMEM) has roughly twice the concentration of amino acids and four
times the amount of vitamins as EMEM, as well as ferric nitrate, sodium pyruvate, and some supplementary
amino acids (though not all nonessential amino acids). The original formulation contained 1,000 mg/L of
glucose, but in the more commonly used variations this amount was increased to 4,500 mg/L.
ATCC DMEM (ATCC No. 30-2002) has 4,500 mg/L of glucose and a reduced sodium bicarbonate
concentration (1,500 mg/L) for use with 5% CO.
Iscoves Modified Dulbeccos Medium (IMDM) was formulated for growth of lymphocytes and hybridomas.
Compared to DMEM, it has additional amino acids, vitamins and inorganic salts. Potassium nitrate was
substituted for ferric nitrate. It also contains HEPES and selenium. ATCC IMDM (ATCC No. 30-2005) has a
reduced sodium bicarbonate concentration (1,500 mg/L) for use with 5% CO.
Hybri-Care Medium (ATCC No. 46-X) is a combination and modification of DMEM and NCTC 135 medium
supplemented with insulin, oxalacetic acid, and HEPES. It is based on the formulation used by David H.
Sachs and collaborators for the propagation of hybridomas and other fastidious cell lines.
McCoys 5A and RPMI-1640 were developed at Roswell Park Memorial Institute (RPMI) in Buffalo, New York.
McCoys 5A (ATCC No. 30-2007) was originally used to grow Novikoff hepatoma cells and will support the
growth of primary cultures.
RPMI-1640 is a modification of McCoys 5A and was developed for the long-term culture of peripheral blood
lymphocytes. RPMI-1640 will support the growth of a wide variety of cells in suspension as well as a number
of cells grown as monolayers.

ATCC RPMI-1640 (ATCC No. 30-2001) was modified to contain higher amounts of glucose (4,500 mg/L),
sodium pyruvate, and HEPES buffer. It also contains a reduced concentration of sodium bicarbonate (1,500
mg/L) for use with 5% CO.
Hams Nutrient Mixtures were originally developed to support the clonal outgrowth of Chinese hamster
ovary (CHO) cells (ATCC CCL-61). As with EMEM, there have been numerous modifications to the original
formulation including Hams F-12 medium, a more complex formulation than the original F-10 suitable for
serum-free propagation.
Kaighns modification of Hams F-12 (Hams F-12K) was designed to support the growth and differentiation
of primary cells with or without serum. F-12K has increased amounts of amino acids, pyruvate, biotin,
calcium, magnesium, putrescine, and phenol red in addition to other modifications from the F-12 formula.
ATCC Hams F-12K (ATCC No. 30-2004) has a reduced sodium bicarbonate concentration (1,500 mg/L) for
use with 5% CO.
DMEM/F12 Medium is a 1:1 mixture of Dulbeccos modified EMEM and Hams F-12. It is an extremely rich
and complex medium and will support the growth of a broad range of cell types in both serum and serum-
free formulations.
ATCC DMEM/F12 medium (ATCC No. 30-2006) has a reduced sodium bicarbonate concentration (1,500
mg/L) for use with 5% CO.
Leibovitzs L-15 Medium (ATCC No.30-2008) is formulated for use without CO incubation as is found in
teaching laboratories or when collecting biopsy samples. The standard sodium bicarbonate/CO buffering
system is replaced by a combination of phosphate buffers, free-base amino acids, higher levels of sodium
pyruvate, and galactose. Cell cultures can be grown in CO incubators with L-15 medium provided there is
no exchange between the air in the culture vessel with that of the incubator (i.e., caps of flasks are tightly
closed).
Media Formulations
Formulations of media available from ATCC can be found online. Please note that there are cell lines in the
collection that require media not currently sold by ATCC.
Media Ingredients
Sodium bicarbonate and buffering
Cells produce and require small amounts of carbon dioxide for growth and survival. In culture media,
dissolved CO is in equilibrium with bicarbonate ions and many medium formulations take advantage
of this CO/bicarbonate reaction to buffer the pH of the medium. CO dissolves freely into the medium
and reacts with water to form carbonic acid. As the cells metabolize and produce more CO, the pH of the
medium decreases as the chemical reaction below is driven to the right:
HO + CO HCO H+ + HCO
The optimal pH range of 7.2 to 7.4 can be maintained by supplementing the medium with sodium
bicarbonate and regulating the level of CO in the atmosphere above the medium as shown by the reaction
below:
HO + CO + NaHCO H+ + Na+ + 2HCO
In tissue culture, cells are grown either in open systems (where there is free exchange of the atmosphere

immediately above the medium with the atmosphere of the incubator) or in closed systems (where the two
atmospheres are kept separate). The buffering system employed in the medium needs to be matched to the
culture system. Otherwise the cells may be subject to metabolic stress which will impair their performance.
In closed systems the level of CO is regulated by the metabolism of the cells. The culture vessel must
be sealed (flasks tightly capped) to retain any CO generated by the cells. Consequently, closed systems
provide additional protection against contamination and have simpler incubator requirements than open
systems. Closed systems usually require media with buffers based on Hanks balanced salt solution having
relatively low levels of sodium bicarbonate.
In open systems, humidity (to reduce evaporation) and a means of regulating CO levels (if the culture
medium contains sodium bicarbonate) are required during incubation to maintain the pH of the culture
medium. Open systems usually require the higher levels of sodium bicarbonate found in Earles salt solution
combined with a 5 to 10% CO atmosphere supplied by the incubator. In general, 1.2 g/L to 2.2 g/L of
sodium bicarbonate is used with 5% CO whereas 3.7 g/L sodium bicarbonate is used with 10% CO. The
exact amount will depend upon the medium formulation.
In some cases, researchers gas the atmosphere of the culture vessel with a stream of sterile-filtered 5%
CO/95% air mixture and then tightly seal the flask prior to incubation in a nonhumidified and non-CO
incubator. While these culture vessels work with simpler non-humidified, non-CO incubators, the medium
requirements are those of an open system.
All ATCC media, with the exception of Leibovitzs L-15 (ATCC No. 30-2008), are designed to be used with
5% CO levels. Most have a sodium bicarbonate concentration of 1.5 g/L and are supplemented with extra
sodium pyruvate. ATCC modification of McCoys 5A (ATCC No. 30-2007) has a slightly higher levels of
sodium bicarbonate (2.2 g/L) and does not contain sodium pyruvate.
While most commercial formulations of liquid media do contain the appropriate amount of sodium
bicarbonate, it is generally omitted from the powdered form and needs to be added before use. Some
medium formulations incorporate other buffering systems such as phosphate or HEPES in addition to CO/
sodium bicarbonate. These media have the advantage of maintaining optimal pH in an open system when
the culture vessel is removed from the enriched CO atmosphere of the incubator.
HEPES buffer
HEPES and other organic buffers can be used with many cell lines to effectively buffer the pH of the
medium. Indeed, some standard medium formulations include HEPES. However, this compound can be
toxic, especially for some differentiated cell types, so evaluate its effects before use. HEPES has been shown
to greatly increase the sensitivity of media to the phototoxic effects induced by exposure to fluorescent
light.,
Phenol red
Phenol red is used to monitor the pH of media. During cell growth, the medium changes color as it changes
pH due to metabolites released by the cells. At low pH levels, phenol red turns the medium yellow, while
at higher pH levels it turns the medium purple. For most tissue culture work (pH 7.4), the medium should
be bright red.
Unfortunately, phenol red can mimic the action of some steroid hormones, particularly estrogen. For
studies with estrogen-sensitive cells, such as mammary tissue, use media without phenol red. Additionally,
the sodium-potassium ion homeostasis is upset when phenol red is included in some serum-free
formulations; this effect is neutralized by the inclusion of serum or bovine pituitary hormone in the
medium. Phenol red is frequently omitted from studies with flow cytometry as its color interferes with
detection.

L-Glutamine
L-Glutamine (ATCC No. 30-2214) is an essential amino acid required by virtually all mammalian and insect
cells grown in culture. It is used for protein production, as an energy source, and in nucleic acid metabolism.
It is also more labile in liquid cell culture media than other amino acids. The rate and extent of L-glutamine
degradation are related to storage temperatures, age of the product, and pH.
Because L-glutamine is so labile, it is often omitted from commercial liquid medium preparations to
lengthen the product shelf life. In these cases, it must be aseptically added prior to use. L-Glutamine is not
as labile in dry form and most powdered medium formulations do include it.
In some cases, the addition of L-glutamine to complete cell culture medium can extend the usable life of the
medium. If L-glutamine is suspected to be a limiting factor during cell culture, a simple test of spiking the
medium with a small amount of L-glutamine will determine whether or not more is required. Simply add
a small amount of L-glutamine (~2 mM final concentration) to the culture medium. If the cell growth rate
increases, L-glutamine is most likely deficient and more should be added. Alternately, the concentration of
L-glutamine can be measured directly by standard analytical means such as HPLC (High Performance Liquid
Chromatography).
L-Glutamine concentrations for mammalian cell culture media can vary from 0.68 mM in Medium 199 to 4
mM in Dulbeccos Modified Eagles Medium. Invertebrate cell culture media, such as Schneiders Drosophila
medium, may contain as much as 12.3 mM L-glutamine.
Use caution when adding more L-glutamine than is called for in the original medium formulation.
L-Glutamine degradation results in the build-up of ammonia which can have a deleterious effect on some
cell lines. For most cell lines, ammonia toxicity is more critical for cell viability than L-glutamine limitation.
Nonessential amino acids
All medium formulations contain the ten essential amino acids as well as cysteine, glutamine, and tyrosine.
The inclusion of the other non-essential amino acids (alanine, asparagine, aspartic acid, glycine, glutamic
acid, proline, and serine) in some media formulations reduces the metabolic burden on the cells allowing
for an increase in cellular proliferation.
Sodium pyruvate
Pyruvate is an intermediary organic acid metabolite in glycolysis and the first component of the Embden-
Meyerhof pathway. It can pass readily into or out of the cell. Its addition to tissue culture medium provides
both an energy source and a carbon skeleton for anabolic processes. Pyruvate may help in maintaining
certain specialized cells, in clonal selection, in reducing the serum concentration of the medium, and
in reducing fluorescent light-induced phototoxicity. Cellular metabolism of pyruvate produces carbon
dioxide which is given off into the atmosphere and becomes bicarbonate in the medium. Sodium pyruvate
is added to give a final concentration of 1 mM in most media, but is increased to 5 mM in Leibovitzs L-15
medium primarily to facilitate use in CO-free environments.
Media Supplements
The complete growth media recommended for some cell lines requires the addition of components not
already available in the base media and serum. These components include hormones, growth factors and
signaling substances that sustain proliferation and maintain normal cell metabolism.
Supplements are usually prepared as 100 (or higher) stock solutions in serum-free medium. Some
supplements may need to be dissolved in a solvent prior to subsequent dilution in serum-free medium
to the stock concentration. Stock concentrations should be aliquoted into small volumes and stored at an

appropriate temperature; most stock concentrations can be stored at 80C, but check with your supplier
prior to storing.
The addition of supplements can change the final osmolality of the complete growth medium, which may
have a negative effect on the growth of cells in culture. It is best to recheck the osmolality of the complete
growth medium after small volumes of supplement stock solutions are added; optimal osmolality for most
vertebrate cell lines should fall between 260 mOSM/kg and 320 mOSM/kg.
After supplements have been added to a base medium, the shelf life of the complete growth medium should
be determined on a case-by-case basis. Complete media containing protein supplements (e.g., epidermal
growth factor, bovine serum albumin, etc.) tend to degrade faster than base media alone. Most complete
growth media can be stored in aliquots at 2C to 8C for about a month. However, if any supplement is
expected to expire before the one-month period has passed, the expiration date for the complete growth
media should follow suit. Some fastidious cell lines may require that components be added immediately
before use. Do not freeze complete growth medium. Freezing cell culture media at 70C or below causes
some of the growth factors and/or vitamins to precipitate out of solution. It can be very difficult to get these
components to go back into solution after thawing, even if warmed to 37C. ATCC recommends storing
media between 2C and 8C, away from light.
For additional information regarding the preparation, storage, or usage of specific supplements, contact
your local supplier or consult with the manufacturers Product Information Sheet.
Osmolality
The osmolality of cell culture media for most vertebrate cells is kept within a narrow range from 260
mOsm/kg to 320 mOsm/kg, even though most established cell lines will tolerate a rather large variation in
osmotic pressure. In contrast, the osmolality requirements for some invertebrate cell lines fall outside of this
range. For example, the snail embryo (ATCC CRL-1494) requires medium of about 155 mOsm/kg, while
some insect cells prefer 360 mOsm/kg to 375 mOsm/kg. Most commercially available liquid media report
osmolality and it is advisable to check the osmolality of any medium after the addition of saline solutions,
drugs or hormones dissolved in an acid or base solution, or large volumes of buffers (e.g., HEPES).
Antibiotics and Antimycotics

Antibiotics and/or antimycotic agents are added to cell culture media as a prophylactic to prevent
contamination, as a cure once contamination is found, to induce the expression of recombinant proteins,
or to maintain selective pressure on transfected cells.
Routine use of antibiotics or antimycotics for cell culture is not recommended unless they are specifically
required, such as G418 for maintaining selective pressure on transfected cells. Antibiotics can mask
contamination by mycoplasma and resistant bacteria. Further, they can interfere with the metabolism of
sensitive cells. Avoid antimycotics as they can be toxic to many cell lines.
While cell lines can be cured of microbial contamination with antibiotics and/or antimycotics, this
is not recommend unless the cell line is irreplaceable; the process is lengthy and there is no guarantee
contamination will be eliminated. Even if the contamination is eliminated, there is no way of ensuring that
the resulting cell line will have the same characteristics as the initial one due to the stress of the treatment.
It is best to discard the cell line and start over with new stocks. Mycoplasma contamination in particular is
very difficult to eliminate. (See page 28) In some cases, antibiotic use for short periods of time can serve as
a valuable prophylactic. For example, antibiotic use is recommended when developing and working with
primary culture and when using flow cytometry to isolate subpopulations.

If an antibiotic is used in medium, penicillin-streptomycin solution (ATCC No. 30-2300) can be added at
0.5 to 1 mL of solution per 100 mL of cell culture medium for a final concentration of 50 to 100 IU/mL
penicillin and 50 to 100 g/mL streptomycin. Gentamicin sulfate, another antibiotic (ATCC No. 30-2303), is
used at 50 to 100 g/mL. The antimycotic amphotericin B (ATCC No. 30-2301) is used at 2.5 g/mL. These
concentrations apply to media that contain serum. For serum-free media, reduce the concentrations by at
least 50%.
Animal Sera
Sera serve as a source for amino acids, proteins, vitamins (particularly fat-soluble vitamins such as A, D, E,
and K), carbohydrates, lipids, hormones, growth factors, minerals, and trace elements. Additionally, serum
buffers the culture medium, inactivates proteolytic enzymes, increases medium viscosity (which reduces
shear stress during pipetting or stirring), and conditions the growth surface of the culture vessel. The exact
composition is unknown and varies from lot to lot, although lot-to-lot consistency has improved in recent
years.
Sera from fetal and calf bovine sources are commonly used to support the growth of cells in culture. Fetal
serum is a rich source of growth factors and is appropriate for cell cloning and for the growth of fastidious
cells. Calf serum, because of its lower growth-promoting properties, is used in contact-inhibition studies
with NIH/3T3 cells (ATCC CRL-1658). In contrast to fetal or calf sera, horse serum is collected from a closed
herd of adult animals ensuring lot-to-lot consistency. Horse serum is less likely to carry the contaminants
found in bovine sera such as viruses and less likely to metabolize polyamines which may be mitogenic
for some cells. Horse and bovine calf sera are less expensive and more readily available than fetal bovine
serum. The pricing and availability of fetal serum fluctuates considerably.
Unfortunately, naturally derived products from bovine sources may contain adventitious viruses such
as bovine viral diarrhea virus (BVDV), bovine parvovirus, bovine adenovirus, and blue tongue virus.
All reputable suppliers test their products for infectious virus by several methods including fluorescent
antibody, cytopathic effect, and hemadsorption. These products are also screened for the standard
microbial contaminants such as bacteria, fungi, and mycoplasma.
BVDV, in contrast to the other virus contaminants, is present in nearly all bovine serum at very low levels
even when tests for infectious virus are negative. Fortunately, very few cell lines (except those of bovine
origin) are susceptible to this virus. For the few sensitive cell lines, use non-bovine sera or irradiated bovine
sera. Several ATCC cell lines were tested for BVDV contamination and the results of this study are indicated
in the cell line description on the website. Bovine-derived products also may contain the agent responsible
for bovine spongiform encephalopathy (BSE). Unfortunately, there is no test for the presence of this agent
and we highly recommend that you obtain all bovine products (including sera) from countries not affected
by BSE such as the United States, Australia and New Zealand.
At one time animal serum was a major source of mycoplasma contamination of tissue culture cells. However,
nearly all sera today are filtered through several 0.1-m pore (or smaller) filters which effectively remove
this organism.
ATCC offers the following four types of animal sera:
Fetal Bovine Serum (also known as fetal calf ) ATCC No. 30-2020
Fetal Bovine Serum qualified for embryonic stem cells ATCC No. SCRR-30-2020
Iron-supplemented Calf Bovine Serum ATCC No. 30-2030
Horse Serum ATCC No. 30-2040
These products are rigorously tested for adventitious infective agents and sourced from only U.S. herds.
Further, each lot is tested for its ability to support cell growth and is the same sera used in ATCC labs.

Storage
Store sera at 20C or colder for storage over 30 days. ATCC sera are routinely stored at 70C. Do not store
sera at temperatures above 20C for any length of time. Avoid repeated freeze-thaws by dispensing and
storing in aliquots.
Thawing
The following procedure is used to thaw serum:
1. Place frozen serum in a refrigerator at 2C to 8C overnight.
2. Put the bottles in a 37C water bath and gently agitate from time to time to mix the solutes that tend to
concentrate at the bottom of the bottle.
Do not keep the serum at 37C any longer than necessary to thaw it, and do not thaw the serum at higher
temperatures. Thawing serum in a bath above 40C without mixing may lead to the formation of a
precipitate inside the bottle.
Turbidity and precipitates
All sera may retain some fibrinogen. Because external factors may initiate the conversion of fibrinogen to
fibrin, flocculent material or turbidity may be observed after serum is thawed. The presence of this material
does not alter the serums performance. If the presence of flocculent material or turbidity is a concern, it can
be removed by filtration through a 0.45-m filter.
A precipitate can form in serum when incubated at 37C or higher for prolonged periods of time which may
be mistaken for microbial contamination. This precipitate may include crystals of calcium phosphate, but
does not alter the performance of the serum as a supplement for cell culture. Heat inactivation of sera can
also cause the formation of precipitates.
Heat inactivation
ATCC does not routinely use heat-inactivated serum unless specifically required for a particular cell line.
Heat inactivation is usually unnecessary and can be detrimental to the growth of some cells. It will reduce
or destroy growth factors present in the serum.
Heat inactivation was originally performed to inactivate complement (a group of proteins present in sera
that are part of the immune response) as well as to destroy mycoplasma contaminants. Today, mycoplasma
contamination, if any, is removed by filtration. Removal of complement is usually unnecessary, but can be
important when preparing or assaying viruses or in cytotoxicity tests. According to a study by HyClone,
warming serum to 37C inactivates heat-labile complement factors. A few types of cell lines grow better in
heat-inactivated sera such as embryonic stem cells and many insect cell lines.
The following procedure can be used to heat-inactivate serum:
1. Thaw serum.
2. Preheat a water bath to 56C. Use sufficient water to immerse the bottle above the level of serum.
3. Mix thawed serum by gentle inversion and place in the 56C bath. The temperature of the water bath
will drop.
4. When the temperature of the water bath reaches 56C again, continue to heat for an additional 30
minutes. Mix gently every 5 minutes to insure uniform heating.
5. Remove serum from water bath, cool quickly (slow cooling can sometimes reverse the inactivation of
complement activity), and store at 20C or colder.

Culture Vessels and Surfaces
Vessels
Culture vessels provide a contamination barrier to protect the cultures from the external environment
while maintaining the proper internal environment. For anchorage-dependent cells, the vessels provide a
suitable and consistent substrate for cell attachment. Other characteristics of vessels include easy access to
the cultures and optically clear viewing surfaces.
Originally all culture vessels were glass. Drawbacks for glass include the heavy weight, expense, labor-
intensive cleaning, and poor microscopic viewing compared to plastic. By the 1960s, surface treatment
techniques were developed for polystyrene, allowing plastic vessels to replace glass for most cell culture
applications.
The information below focuses on standard culture vessels used by many researchers. Large-scale culture
equipment is not included.
Selecting the right vessel
First, match the characteristics of the cells to be grown with the characteristics of the different culturing
systems. There are three basic types of cell cultures:
Anchorage dependent, which must become attached to a surface to grow (for example, human diploid
fibroblasts).
Anchorage independent, which grow in suspension (most blood-derived cell cultures).
Cells that can grow either attached or in suspension (many transformed cell lines such as HeLa and
BHK-21).
Understand the growth requirements of the cultures to help select the best culture system. There are four
basic culture systems:
Stationary monolayer cultures which are grown in undisturbed flasks, dishes, and multiwell plates.
These are the easiest culture systems to use and require the least amount of equipment. However,
these systems are very labor intensive for producing large quantities of cells.
Moving monolayer cultures which are grown primarily in roller bottles. These vessels are slowly rotated
(approximately 0.5 rpm to 1 rpm) on motorized racks or drums and are widely used for producing
large quantities of cells. Roller bottles employ simple technology but require an investment in the
appropriate equipment.
Stationary suspension cultures which are grown without agitation in untreated dishes and flasks. These
are best for growing small volumes of anchorage-independent cells that grow poorly in traditional
stirred suspension cultures.
Moving suspension cultures which are grown in mechanically stirred vessels (spinner flasks), bioreactors,
or fermentors. These systems are the most economical in terms of space, labor and media; as a result,
stirred suspension cultures are usually the method of choice for producing large volumes of cells both
in the lab and in industry. Many anchorage-dependent cells can be adapted to grow on microcarriers
to take advantage of these systems.
Next, decide whether the cells will be grown as an open system or as a closed system (see the section on
sodium bicarbonate, page 14). Open-system plastic dishes are less expensive than closed-system flasks,
but require more expensive incubators that can regulate the CO and humidity in the atmosphere. Closed

systems provide additional protection against contamination and have simpler incubator requirements.
All dishes and multiwell plates are open systems. All other culture vessels can be used in either mode by
leaving caps loose for an open system or tightened for a closed system. The plastic walls of culture vessels
are slightly permeable to carbon dioxide and oxygen, permitting a very small amount of gas exchange.
This is not a problem in most culture applications, but may interfere with anoxia experiments or long-term
storage of media. Caps that allow gas exchange when the cap is fully tightened are available to reduce
opportunities for flask spills and contamination in open systems.
The last step is matching the desired cell yield with an appropriately sized culture vessel. For monolayer
cultures, the yield is limited by the area of treated growth surface. Approximately 0.5 10 cells/cm to
1 10 cells/cm of treated surface is a typical yield for confluent continuous mammalian cell lines. For
suspension cultures the total cell yield is determined by the working volume of the vessel. In stirred systems,
cell concentrations can easily reach between 1 10 cells/mL and 2 10 cells/mL of medium. However,
the exact yields will need to be determined empirically for each cell line. ATCC strongly recommends that
cells be maintained in the logarithmic phase of growth, and not be allowed to enter the stationary phase.
Anchorage-dependent cell lines are routinely passaged or split before they reach confluency.
Flasks
Alexis Carrel developed the first glass flasks in the 1920s. Harry Earle developed the more traditional straight
neck rectangular (also hexagonal) glass T-flasks in the 1940s. Today, plastic flasks are available with a range
of growing areas, a variety of shapes, with several different neck designs. Choice of design depends on the
cell culture techniques used as well as personal preference. The more common sizes are listed below.
Description Growth area (cm) Recommended working Cell yield*

volume (mL)
T-25 25 5 to 10 2.5 10
T-75 75 15 to 25 7.5 10
T-150 150 30 to 50 15.0 10
T-175 175 35 to 60 17.5 10
T-225 225 45 to 75 22.5 10
*Cell line dependent. Based upon a density of 1 10 cells/cm.
Cell culture dishes

Cell culture dishes offer the best economy and access to the growth surface.
This makes them the vessels of choice for cloning or other manipulations such
as scraping that require direct access to the cell monolayer. They must be used
with incubators that control CO and humidity. Most manufacturers offer
dishes in four diameters: 35 mm, 60 mm, 100 mm, and 150 mm. These are
nominal diameters and may not be the actual diameter of the growth surface.
Cell culture dishes are available with either specially treated surfaces for
growing anchorage-dependent cells, or untreated (native) surfaces for
growing suspension cultures where attachment is not desired.
Description Growth area (cm) Working volume (mL) Cell yield*

35 8 1 to 2 0.8 10
60 21 4 to 5 2.1 10
100 55 10 to 12 5.5 10
150 148 28 to 32 14.8 10

Multiwell plates
These widely used vessels were originally designed for virus titration, but have since become popular in
many other applications, especially hybridoma production, high-throughput screening, and toxicity
testing. Multiwell plates offer significant savings in space, media, and reagents when compared to an equal
number of dishes. They are more convenient to handle, especially if the pipettors, plate washers, readers,
and other equipment for processing these plates are used. They must be used with incubators that control
humidity and CO levels.
Description Growth well (cm) Working volume/ well (mL) Cell yield*
96-well 0.32 0.1 to 0.2 0.32 10
48-well 1.00 0.3 to 0.6 0.8 10
24-well 1.88 0.5 to 1.2 1.9 10
12-well 3.83 1.0 to 2.4 3.8 10
6-well 9.40 2.0 to 3.0 9.5 10
Roller bottles
The roller bottle was developed for cultivating large numbers of anchorage-dependent cells. Today they
provide a more economical means for cultivating large volumes of cells using essentially the same culture
techniques as with flasks but with considerably less labor. Besides the traditional smooth wall design, roller
bottles are available with small ridges that approximately double the surface area available for growing
cells without increasing the dimensions of the bottles.
Description Growth area (cm) Working volume (mL) Cell yield*

Small 490 100 to 150 4.9 10
Standard 850 170 to 250 8.5 10
Pharmaceutical 1750 340 to 500 17.5 10
Surface Coatings and Feeder Cells

Most tissue culture work uses disposable polystyrene
vessels. The vessel surface is treated to render it
hydrophilic (wettable). Most cell lines in the ATCC
collection are cultivated on treated plastic surfaces in
dishes, flasks, or roller bottles. Since the properties of
tissue culture plastic can vary among manufacturers,
samples should be evaluated for their ability to support
cell growth and propagation prior to use. ATCC routinely
uses the SelecT fully automated cell culture system.
Some fastidious cell lines require further treatment of the
growth surface before they will attach and proliferate.
The most common techniques include coating the
surface with serum, collagen, laminin, gelatin (ATCC No. Human stem cell colony on Mitomycin C treated
neonatal human fibroblast cells.
PCS-999-027), poly-L-lysine, or fibronectin.
Beyond simple attachment, some cells require specialized surface treatment in order for them to differentiate
into more tissue-like formations. For example, endothelial cells will form tubules and neuronal cells will

extend neurite processes when cultured on a surface of extracellular matrix (ECM) proteins (ATCC No. ACS-
3035). These ECM proteins closely resemble the basal lamina membrane surrounding cells in tissue and
not only provide attachment points, but modulate signal transduction from external growth factors and
hormones, influence the permeability of ions and nutrients, and actively communicate with intracellular
processes through integrins.
Finally, some cells, particularly when seeded at low densities as for cloning, require the support of living
cells. Most cells are happier in a crowd. Feeder layer cells supply a crowd by conditioning the medium
through metabolic leakage and/or the active secretion of growth and other factors. They also provide a
support matrix for cell attachment and proliferation. To prevent feeder layer cells from overgrowing the
cells of interest, they are treated to prevent division. Common methods include irradiation with X-rays or
gamma rays or treatment with mitomycin C (ATCC No. SCRR-3020). Each of these treatments damages
cellular DNA so that the cells continue to metabolize but can no longer proliferate. ATCC offers a variety of
well-characterized feeder cells.
ATCC No. Product Name Description

CRL-2581 C166 Mouse embryonic endothelial cells
CRL-2583 C166GFP Mouse embryonic endothelial cells with GFP expression
CRL-2749 OP9 Mouse embryonic bone marrow stromal cells
48-X IRR-3T3 Irradiated 3T3 cells (mouse embryonic fibroblast)
55-X IRR-MRC-5 Irradiated MRC-5 cells (human diploid lung fibroblast)
SCRC-1007 AFT024 Mouse embryonic liver fibroblasts
SCRC-1007.1 Irradiated AFT024 Irradiated mouse embryonic liver fibroblasts
SCRC-1008 MEF (C57BL/6) Mouse embryonic fibroblasts
SCRC-1008.1 MEF (C57BL/6) IRR Irradiated mouse embryonic fibroblasts
SCRC-1040 MEF (CF-1) Mouse embryonic fibroblasts
SCRC-1040.1 MEF (CF-1) IRR Irradiated mouse embryonic fibroblasts
SCRC-1040.2a MEF (CF-1) MITC Mitomycin C treated mouse embryonic fibroblasts
SCRC-1041 HFF-1 Human foreskin fibroblasts
SCRC-1041.1 HFF-1 IRR Irradiated human foreskin fibroblasts
SCRC-1045 MEF (DR4) Multidrug resistant mouse fibroblasts
SCRC-1049 SNL76/7 STO fibroblasts with G418 resistance and endogenous expression of LIF
STO fibroblasts with resistance to G418 and puromycin plus
SCRC-1050 SNLP 76/7-4
endogenous expression of LIF
Dermal Fibroblasts;
Normal, Human,
PCS-201-011 Mitomycin C treated neonatal human fibroblast cells
Neonatal, Mitomycin C
Treated

Cryopreservation
Cryopreservation
Most cell cultures can be stored for many years, if not indefinitely, at temperatures below 130C
(cryopreservation). ATCC has recovered cells from cultures cryopreserved for more than 40 years. The many
advantages of cryopreservation far outweigh the required investment in equipment and reagents. These
advantages include:
Generation of safety stocks to ensure against loss of the culture from equipment failures or
contamination by microorganisms or other cell lines.
Elimination of the time, energy, and materials required to maintain cultures not in immediate use.
Preservation of cells with finite population doublings (that will ultimately senesce).
Insurance against phenotypic drift in the culture due to genetic instability and/or selective pressure.
Creating a standard reagent to be used for a series of experiments.
Overview
As the cell suspension is cooled below the freezing point, ice crystals form and the concentration of the
solutes in the suspension increases. Intracellular ice can be minimized if water within the cell is allowed to
escape by osmosis during the cooling process. A slow cooling rate, generally 1C per minute, facilitates this
process. However, as the cells lose water, they shrink in size and will quickly lose viability if they go beyond
a minimum volume. The addition of cryoprotectant agents such as glycerol or dimethylsulfoxide (DMSO)
will mitigate these effects.
The standard procedure for cryopreservation is to freeze cells slowly until they reach a temperature below
70C in medium that includes a cryoprotectant. Vials are transferred to a liquid-nitrogen freezer to maintain
them at temperatures below 130C.
The recovery of cryopreserved cells is straightforward: Cells are thawed rapidly in a water bath at 37C,
removed from the freeze-medium by gentle centrifugation and/or diluted with growth medium, and
seeded in a culture vessel in complete growth medium.
There are numerous factors which affect the viability of recovered cells. Modify the procedure for each cell
line to attain optimal cell viability upon recovery. Some of the critical parameters for optimization include
the composition of the freeze medium, the growth phase of the culture, the stage of the cell in the cell cycle,
and the number and concentration of cells within the freezing solution.
ATCC provides information on cryopreservation for all cell lines on the Product Sheet. Most ATCC cell lines
are frozen with a cryopreservation medium consisting of 5% DMSO and complete growth medium.
Freeze Medium
Glycerol and DMSO at 5% to 10% are the most common cryoprotectant agents. While DMSO can be toxic
to cells, it penetrates them much faster than glycerol and yields more reproducible results. Unfortunately,
DMSO can cause some cells to differentiate (e.g., HL-60 promyeloblast cells) and may be too toxic for some
cells (e.g., HBE4-E6/E7 lung epithelial cells). Glycerol should be used in these instances. Glycerol can be
sterilized by autoclaving whereas DMSO must be sterilized by filtration. Care should be used when handling
any DMSO solution as it will rapidly penetrate intact skin and may carry toxic contaminants along with it.
Use only reagent-grade (or better, such as cell culture-grade) DMSO or glycerol. Store both in aliquots

Cryopreservation
protected from light. ATCC offers DMSO (ATCC No. 4-X) that has been thoroughly tested for cell culture use.
For cells grown in serum-free medium, adding 50% conditioned medium (serum-free medium in which the
cells were grown for 24 hours) to both the cell freezing and the recovery medium may improve recovery
and survival. The addition of 10% to 20% cell culture-grade bovine serum albumin to serum-free freezing
medium may also increase postfreeze survival.
Serum-free freezing media have also been developed. ATCC Serum-Free Cell Freezing Medium (ATCC
No. 30-2600) can be used for both cells cultured in serum-supplemented growth medium as well as cells
grown under serum-free conditions. This proprietary formulation contains 10% DMSO and methylcellulose
is suitable for the cryopreservation of adherent and suspension cell cultures. Cells cryopreserved using
Serum-Free Freezing Medium show levels of viability and percent attachment (adherent cells) that are
comparable to cells preserved in DMSO and FBS. (See: Figure 3)
Viability Attachment
90% 120%
85%
83% 82%
80% 77%
75% 100% 100%
71% 100%
70% 69% 92%
66%
83%
60% 80%
Percent Adhesion
Percent Viabilit y
50% 62%
60%
40%
30% 40%
33%
20% 22%
20%
10% 10%
0%
0% CCL 163 3 T3 CCL 81 VER O CCL 23 HEp- 2C CL 26 BSC- 1
CCL 163 3 T3 CCL 81 VER O CCL 23 HEp- 2 CCL 26 BSC-1
Cell Lin e Cell Lin e
Serum-Free Cell Freezing Medium Freezing Me dium wit h FBS
Serum-Free Cell Freezin g Medium Freezing Med ium with FBS
Figure 3. Cells cryopreserved using ATCC Serum-Free Cell Freezing Medium show levels of
viability and percent attachment that are comparable to cells preserved in DMSO and FBS.
Other variations of freeze medium formulations include high (up to 90%) concentrations of serum which
presumably supplies some cryoprotection as well as additional growth factors; use of a balanced salt
solution designed for hypothermal conditions in place of medium designed for 37C incubation; and the
addition of apoptotic inhibitors which may prevent delayed onset cell death following recovery. Optimum
formulations for individual cell lines need to be determined empirically.
Equipment
Cryopreservation vials
There are two materials to choose from for cryopreservation vials: glass or plastic. Glass
vials are more difficult to work with; they need to be sterilized before use, they do
not come with labels (information is imprinted into the glass), they need to be sealed
with a hot flame, and they can be difficult to open. However, they are preferred for
long-term storage (many years) of valuable cultures and are considered fail-safe once
properly sealed. ATCC uses glass vials for the storage of seed stocks which are placed
in the lower level of the liquid nitrogen tank. Plastic vials are used for the storage of
distribution stocks.
Plastic vials come in two varieties: those with an internal thread and silicone gasket and those with an external
thread. The internal-thread version was the first commercially available, but has some disadvantages over
the external-thread version. For example, while the silicone gasket provides an excellent seal, it needs to be
tightened just right; too tight or too loose and the vial will leak.

Cryopreservation
Controlled-rate freezing chambers
There are several means to achieve a cooling rate of 1C per minute. The best is with a computer controlled,
programmable electronic freezing unit (such as CryoMed Freeze) which rigorously maintains this rate of
cooling. This is the method used exclusively at ATCC. Such equipment is relatively expensive and absolutely
necessary for only the most sensitive cells.
A less costly approach is to place the cryopreservation vials into an insulated chamber and cool for 24
hours in a mechanical freezer at 70C or lower. There are several commercially available freezing chambers
which achieve a cooling rate very close to the ideal 1C per minute (Mr. Frosty, Nalgene No. 5100-0001;
or StrataCooler, Agilent Technologies No. 401349). Alternately, the vials can be placed into a polystyrene
box with 15-mm (3/4 inch) thick walls and 1L capacity packed with paper, cotton wool, or foam peanuts for
insulation.
Liquid Nitrogen Freezer Storage

The ultra-low temperatures (below 130C) required for long-term storage can be maintained by specialized
electric freezers or more commonly by liquid nitrogen freezers. There
are two basic types of liquid nitrogen storage systems: immersing
vials in the liquid and holding vials in the vapor phase above the
liquid. The liquid-phase system holds more nitrogen and thus
requires less maintenance. However, there is always a chance that
some liquid will enter improperly sealed vials which may explode
when retrieved. For this reason ATCC strongly recommends storage
in vapor-phase systems.
Vapor-phase systems create a vertical temperature gradient within
the container. The temperature in the liquid nitrogen at the bottom
will be 196C, whereas the temperature at the top will vary depending upon the amount of liquid nitrogen
at the bottom as well as the amount of time the container is opened. To ensure safe storage of cells, be sure
to keep enough liquid nitrogen in the container so that the temperature at the top is 130C or colder. All
storage systems should be equipped with temperature alarms.
Cryopreservation Procedure
The procedure below will work for most cell cultures and should be modified as needed. Freeze medium
formulations for all ATCC cell lines are provided on the Product Sheet. Harvest cells in exponential growth.
1. Check your cell culture for contamination from bacteria, fungi, mycoplasma, and viruses (see
Contamination, page 28) immediately before cryopreservation. In most cases, the results of the
contamination screen will be available some time after the cultures are cryopreserved (10 to 14 days).
If contamination is confirmed, then destroy the frozen material.
2. Prepare a freeze medium consisting of complete growth medium and 5% DMSO (ATCC No. 4-X). Do
not add undiluted DMSO to a cell suspension as dissolution of DMSO in aqueous solutions gives off
heat.
3. Collect cells by gentle centrifugation (10 minutes at 125 g) and resuspend them in the freeze medium
at a concentration of 1 10 to 5 10 viable cells/mL. Continue to maintain the cells in culture until the
viability of the recovered cells is confirmed (see Step 9).
4. Label the appropriate number of vials with the name of the cell line and the date. Then add 1 to 1.8 mL
of the cell suspension to each of the vials (depending upon the volume of the vial) and seal.

Cryopreservation
5. Allow cells to equilibrate in the freeze medium at room temperature for a minimum of 15 minutes but
no longer than 40. This time is usually taken up in dispensing aliquots of the cell suspension into the
vials. After 40 minutes, cell viability may decline due to the DMSO.
6. Place the vials into a pre-cooled (4C), controlled-rate freeze chamber and place the chamber in
a mechanical freezer at 70C (or colder) for at least 24 hours. Alternately, use a pre-cooled (4C)
programmable freezer unit set to cool the vials at 1C per minute until a temperature below 40C is
achieved and then set to abruptly drop to 130C.
7. Quickly transfer the vials to a liquid nitrogen or 130C freezer. Frozen material will warm up at a rate of
10C per minute and cells will deteriorate rapidly if warmed above 50C.
8. Record the location and details of the freeze.
9. After 24 hours at 130C, remove one vial, restore the cells in culture medium, and determine their
viability and sterility.
Recovery of Cryopreserved Cells

The cell solution in the frozen vial needs to be warmed as rapidly as possible and then immediately combined
with complete culture medium and seeded into an appropriate flask. While cells grown in monolayers can
be recovered from cryopreservation in multiwell plates, the results are not as consistent as with flasks.
Some cell lines, such as hybridoma cultures, take several days before they fully recover from cryopreservation.
Some hybridomas show low viability on the first day in culture and will generate cellular debris. Viability for
most cells declines and reaches a nadir at 24 hours post-thaw. Most, if not all, of this decline appears to be
due to apoptosis (as opposed to necrosis) induced by the stress of the cryopreservation process. After this
time point, cells begin to recover and enter exponential growth.
1. Prepare a culture vessel (T-75 flask) so that it contains at least 10 mL of the appropriate culture medium
equilibrated for temperature and pH.
2. Remove the vial from the liquid nitrogen freezer and thaw by gentle agitation in a 37C water bath (or a
bath set at the normal growth temperature for that cell line). Thaw rapidly until ice crystals have melted
(approximately 2 minutes).
3. Remove the vial from the water bath and decontaminate it by dipping in or spraying with 70% ethanol.
Follow strict aseptic conditions in a laminar flow tissue culture hood for all further manipulations.
4. Unscrew the top of the vial and transfer the contents to a sterile centrifuge tube containing 9 mL
complete growth medium. Remove the cryoprotectant agent by gentle centrifugation (10 minutes at
125 g). Discard the supernatant, taking care not to disturb the soft pellet, and resuspend the cells in
1 mL or 2 mL of complete growth medium. Pipette gently to loosen the pellet and break apart clumps.
(If the cells normally grow as clusters, avoid over-pipetting during resuspension.) Transfer the cell
suspension into the medium in the culture vessel and mix thoroughly.
5. Examine the cultures after 24 hours and subculture as needed.

Contamination and Biosafety

Contamination of cells in culture can arise from many sources including other cell lines, reagents, supplies
such as pipettes and culture vessels, equipment such as tissue culture hoods and incubators, and laboratory
personnel. While the potential for contamination is constant, the risk can be reduced or eliminated by
proper precautions: using only reagents of known quality and sterility, quarantining new cell lines until they
are tested to be free from contamination, performing routine maintenance and cleaning of all equipment,
and properly training cell culture personnel.
Check for Microbial Contamination

When most bacterial contamination occurs, it usually occurs within a few days and is typically obvious to
the naked eye. Distinct changes to the medium such as turbidity, presence of particles visible in suspension,
and a rapid decline in pH (yellow color, indicating acidity) are all indicators of bacterial contamination.
Fastidious bacteria species that grow very slowly can be difficult to detect.
Fungal contaminants may or may not cause a change in the pH of the medium and can be distinguished
from bacteria by checking for the presence of filamentous structures in the suspension. Yeast cells are larger
than bacteria, but may not appreciably change the pH of the medium, and will appear as separate round
or ovoid particles. Microbacterial media which can be used to test for bacterial and fungal contamination
include blood agar, thioglycollate broth, tryptic soy broth, BHI broth, Sabouraud broth, YM broth, and
nutrient broth with 2% yeast extract. However, some microbial contamination is not apparent. For
example, the use of antibiotics can suppress bacterial growth and thus mask contamination. Some viral
infections do not alter the morphology of the cells, and detection of mycoplasma contamination requires
specific assays.
Mycoplasma Contamination
Cell lines are screened for mycoplasma
contamination by direct (agarose and broth
culture) and indirect (Hoechst) methods.,
For example, the fluorochrome Hoechst DNA
stain will bind to the DNA of mycoplasma and
the organisms can be detected easily when Hoechst 33342 staining of an Hoechst 33342 staining of a
examined using a microscope equipped uncontaminated cell culture. contaminated cell culture.
with appropriate fluorescence optics. The
direct culture method requiring both broth and agar will permit isolation of cultivable strains as apparent
by appearance of characteristic mycoplasma colonies on the agar medium.
Both direct and indirect methods for detection of mycoplasma are used at ATCC several times while a cell
line is expanded for the preparation of the token, seed and distribution stocks.
Most cell culture laboratories have incorporated PCR-based mycoplasma testing, using kits such as ATCCs
Unversal Mycoplasma Detection Kit (ATCC No. 30-1012K) into their routine cell culture operations.
Cell cultures can be submitted to the ATCC Mycoplasma Testing Service. See the ATCC Services section of
the website for details.

Treating for Microbiobial Contamination
Eliminating contamination from a cell line is time consuming and does not always work. Discarding the
culture and starting over is preferred. However, if the cells are unique and irreplaceable, one should first
identify the contaminant and select a suitable antibiotic for treatment. It is best to test the contaminating
microbe for its antibiotic sensitivity prior to treatment; this allows for a shorter treatment time and limits
exposure of the cell line to potentially damaging reagents.
The cells are cultured for 1 to 2 weeks in the presence of the antibiotic, and then cultured without antibiotic
for 1 to 2 months. At this point, the line should be retested with a very sensitive test method to make
sure that the culture is clean. Periodic retesting should be employed to make sure that the contaminant
does not reappear. Since antibiotics may be toxic to cells, a selected population that no longer exhibits
qualities of the parental line may result. It may be necessary to examine the cured culture to determine if it
is sufficiently similar to the original line.
Cellular Cross-Contamination
Cross-contamination of one cell line with another can sometimes lead to the replacement of the original cell
with the contaminant, particularly when the contaminant grows faster than the original line. HeLa cells are
perhaps the most famous example of a cross- contaminating cell line overtaking and then masquerading
as the original.
In the 1950s and 1960s, many continuous lines were unknowingly cross-contaminated with other cell lines
including HeLa cells. In the 1970s and 1980s, as many as one in three cell lines deposited in cell repositories
were imposters. This cross-contamination was only uncovered with the development of suitable genetic
markers beginning in 1967. Indeed, several unique cell lines in ATCCs collection turned out to be HeLa
cells upon further study. Despite the confirmation of their HeLa cell origin, cytogenetic analysis suggests
that there are differences among these HeLa-derived cell lines. Several of them possess unique properties.
However, these cell lines should not be used as functional models of their claimed tissues of origin.
More recently, ATCC and other cell repositories have used DNA polymorphisms in addition to enzyme
polymorphisms, HLA typing, and karyotyping to confirm the identity of their cell lines. One of the most
reliable methods to study DNA polymorphisms is the profiling of short tandem repeats (STR) by PCR
Figure 4. STR profiles for two unrelated human cell lines. Top: KU812E (ATCC CRL-2100). Bottom: MRC-5 (ATCC CCL-171). Ampli-
cons were generated using Promegas PowerPlex platform, separated by capillary electrophoresis and analyzed using GeneMap-
per software from Life Technologies.

amplification followed by capillary electrophoresis. STR profiles for all ATCC human cell lines are available
on the website in the catalog descriptions. (See: Figure 4)
Test cell cultures on a regular basis to ensure the absence of contamination from both microorganisms as
well as from other cell lines. If contamination is found, discard the culture and start fresh with a new stock.
Biosafety
The need for precautions when experimenting with cells in culture depends upon the source and nature
of the biological material, the experimental procedure, and the laboratory/containment conditions. Since
every situation is different, the risks need to be identified and appropriate precautions need to be taken
before any work begins.
More information on risk assessment and precautions can be found in the Center for Disease Control (CDC)
publication Biosafety in Microbiological and Biomedical Laboratories, (BMBL) 5th Edition. The text of this
publication is available in its entirety online (http://www.cdc.gov/biosafety/publications/bmbl5/BMBL.
pdf ). Information on agent risk assessment and a description of the four biosafety levels can be found in
this publication.
ATCC assigns a biosafety level (BSL) to each cell line for purposes of packaging for safe shipment. When a cell
line is known to contain an etiologic agent, ATCC classification is at least comparable to the BSL assigned
to the agent by the CDC and in some cases the ATCC designation is more restrictive. ATCC follows federal
biosafety guidelines and takes several factors into consideration when assessing potential hazard.
Biosafety Level 1
Cell lines with animal origin not included under Biosafety Level 2
Biosafety Level 2
Cell lines that harbor mycoplasma or any other BSL 2 agent (See: NOTE)
NOTE:
Cell lines exposed to or transformed by a primate oncogenic virus Some patent cell lines at ATCC are
known to be contaminated with
Primate cell lines that contain viruses mycoplasma and are noted as such
Cell lines carrying a part of certain viral genomes, even if whole virus is in the catalog.
not released from the cell
As the recipient of a cell line, take into account not only the nature of the material but also the
manipulations employed during its handling when assessing the potential laboratory risk. For example,
procedures involving large volumes of cell lines that contain HIV or that include manipulation of HIV in high
concentration should be conducted under BSL 3 conditions.
It is not possible to screen cell lines for the presence of every agent. For added precaution, ATCC handles
all cell lines under BSL 2 practices, even those classified as BSL 1. It is prudent to treat all mammalian cell
lines as potentially hazardous.

Glossary
Glossary Cell strain. A cell strain is derived either from a primary culture
or a cell line by the selection or cloning of cells having specific
properties or markers. In describing a cell strain, its specific
features must be defined. The terms finite or continuous are
The following glossary was originally published by the Tissue to be used as prefixes if the status of the culture is known. If
Culture Association Terminology Committee in 1990. not, the term strain will suffice. In any published description
of a cell strain, one must make every attempt to publish the
Anchorage-dependent cells or cultures. Cells, or cultures
characterization or history of the strain. If such has already
derived from them, which will grow, survive, or maintain
been published, a reference to the original publication must
function only when attached to a surface such as glass or
be made. In obtaining a culture from another laboratory, the
plastic. The use of this term does not imply that the cells are
proper designation of the culture, as originally named and
normal or that they are not neoplastically transformed.
described, must be maintained and any deviations in cultivation
Aneuploid. The situation in which the nucleus of a cell does from the original must be reported in any publication.
not contain an exact multiple of the haploid number of
Chemically defined medium. A nutritive solution for culturing
chromosomes, one or more chromosomes being present in
cells in which each component is specifiable and, ideally, is of
greater or lesser number than the rest. The chromosomes may
known chemical structure.
or may not show rearrangements.
Clone. In animal cell culture terminology, a population of cells
Aseptic technique. Procedures used to prevent the
derived from a single cell by mitoses. A clone is not necessarily
introduction of fungi, bacteria, viruses, mycoplasma, or other
homogeneous and therefore the terms clone and cloned do
microorganisms in cell, tissue, and organ cultures. Although
not indicate homogeneity in a cell population, genetic or
these procedures are used to prevent microbial contamination
otherwise.
of cultures, they also prevent cross-contamination of cell
cultures as well. Cloning efficiency. The percentage of cells plated (seeded,
inoculated) that form a clone. One must be certain that the
Attachment efficiency. The percentage of cells plated (seeded,
colonies formed arose from single cells in order to properly use
inoculated) which attach to the surface of the culture vessel
this term. (See colony forming efficiency.)
within a specified period of time. The conditions under which
such a determination is made should always be stated. Colony forming efficiency. The percentage of cells plated
(seeded, inoculated) that form a colony.
Autocrine cell. In animals, a cell which produces hormones,
growth factors, or other signaling substances for which it also Contact inhibition of locomotion. A phenomenon
expresses the corresponding receptors. (See also endocrine and characterizing certain cells in which two cells meet, locomotory
paracrine.) activity diminishes and the forward motion of one cell over the
surface of the other is stopped.
Cell culture. Term used to denote the maintenance or
cultivation of cells in vitro including the culture of single cells. Continuous cell culture. A culture which is apparently capable
In cell cultures, the cells are no longer organized into tissues. of an unlimited number of population doublings, often referred
to as an immortal cell culture. Such cells may or may not
Cell generation time. The interval between consecutive
express the characteristics of in vitro neoplastic or malignant
divisions of a cell. This interval can best be determined, at
transformation. (See also immortalization.)
present, with the aid of cinephotomicrography. This term is not
synonymous with population doubling time. Crisis. A stage of the in vitro transformation of cells. It is
characterized by reduced proliferation of the culture, abnormal
Cell hybridization. The fusion of two or more dissimilar cells
mitotic figures, detachment of cells from the culture substrate,
leading to the formation of a synkaryon.
and the formation of multinucleated or giant cells. During this
Cell line. A cell line arises from a primary culture at the time of the massive cultural degeneration, a small number of colonies
first successful subculture. The term implies that cultures from usually, but not always, survives and gives rise to a culture with
it consist of lineages of cells originally present in the primary an apparent unlimited in vitro lifespan. This process was first
culture. The terms finite or continuous are used as prefixes described in human cells following infection with an oncogenic
if the status of the culture is known. If not, the term line will virus (SV40). See also cell line, in vitro transformation, and in vitro
suffice. The term continuous line replaces the term established senescence.
line. In any published description of a culture, one must make
Cryopreservation. Ultra-low temperature storage of cells,
every attempt to publish the characterization or history of the
tissues, embryos, or seeds. This storage is usually carried out
culture. If such has already been published, a reference to the
using temperatures below 100C.
original publication must be made. In obtaining a culture from
another laboratory, the proper designation of the culture, as Density-dependent inhibition of growth. Mitotic inhibition
originally named and described, must be maintained and any correlated with increased cell density.
deviations in cultivation from the original must be reported in
any publication.

Glossary
Differentiated. Cells in culture that maintain all or much of system demonstrating form and function typical of the cells in
the specialized structure and function typical of the cell type vivo would be said to be histiotypic.
in vivo.
Homokaryon. A cell possessing two or more genetically
Diploid. The state of the cell in which all chromosomes, except identical nuclei in a common cytoplasm, derived as a result of
sex chromosomes, are two in number and are structurally cell-to-cell fusion.
identical with those of the species from which the culture was
derived. Hybridoma. The cell which results from the fusion of an
antibody- producing tumor cell (myeloma) and an antigenically
Electroporation. Creation by means of an electrical current stimulated normal plasma cell. Such cells are constructed
of transient pores in the plasmalemma usually for the purpose because they produce a single antibody directed against
of introducing exogenous material, especially DNA, from the the antigen epitope which stimulated the plasma cell. This
medium. antibody is referred to as a monoclonal antibody.
Embryo culture. In vitro development or maintenance of Immortalization. The attainment by a cell culture, whether by
isolated mature or immature embryos. perturbation or intrinsically, of the attributes of a continuous
cell line. An immortalized cell is not necessarily one which is
Embryogenesis. The process of embryo initiation and neoplastically or malignantly transformed.
development.
In vitro senescence. The inability of a vertebrate cell culture to
Endocrine cell. In animals, a cell which produces hormones, grow beyond a finite number of population doublings. Neither
growth factors or other signaling substances for which the invertebrate nor plant cell cultures exhibit this property.
target cells, expressing the corresponding receptors, are
located at a distance. (See also autocrine or paracrine.) In vitro transformation. A heritable change occurring in cells
in culture, either intrinsically or from treatment with chemical
Epithelial-like. Resembling or characteristic of, or having the carcinogens, oncongenic viruses, irradiation, transfection
form or appearance of, epithelial cells. In order to define a cell with oncogenes, etc., which leads to the acquisition of altered
as an epithelial cell, it must possess characteristics typical of morphological, antigenic, neoplastic, proliferative, or other
epithelial cells. Often one can be certain of the histologic origin properties. This expression is distinguished from in vitro
and/or function of the cells placed into culture and, under these neoplastic transformation in that the alterations occurring
conditions, one can be reasonably confident in designating the in the cell population may not always include the ability of
cells as epithelial. The individual reporting on such cells should the cells to produce tumors in appropriate hosts. The type of
use as many parameters as possible in assigning this term to a transformation should always be specified in any description.
culture. Until a rigorous definition is possible, it is more correct
to use the term epithelial-like. Organ culture. The maintenance or growth of organ primordia
or the whole or parts of an organ in vitro in a way that may
Euploid. The situation in which the nucleus of a cell contains allow differentiation and preservation of the architecture and/
exact multiples of the haploid number of chromosomes. or function.
Feeder layer. A layer of cells (usually irradiated or mitomycin-C Paracrine. In animals, a cell which produces hormones, growth
treated) that are nondividing but metabolically active, upon factors or other signaling substances for which the target
which a fastidious cell type is cultured. cells, expressing the corresponding receptors, are located in
Finite cell culture. A culture which is capable of only a limited its vicinity, or in a group adjacent to it. (See also autocrine and
number of population doublings after which the culture ceases endocrine.)
proliferation. (See in vitro senescence.) Passage. The transfer or transplantation of cells, with or without
Heterokaryon. A cell possessing two or more genetically dilution, from one culture vessel to another. It is understood
different nuclei in a common cytoplasm, usually derived as a that any time cells are transferred from one vessel to another, a
result of cell-to-cell fusion. certain portion of the cells may be lost, and therefore dilution
of cells, whether deliberate or not, may occur. This term is
Heteroploid. A culture whose cells contain chromosome synonymous with subculture.
number other than the diploid number. This is a term used
only to describe a culture and is not used to describe individual Passage number. The number of times the cells in the culture
cells. Thus, a heteroploid culture would be one which contains have been subcultured or passaged. In descriptions of this
aneuploid cells. process, the ratio or dilution of the cells should be stated so
that the relative cultural age can be ascertained.
Histiotypic. The in vitro resemblance of cells in culture to a
tissue in form, function, or both. For example, a suspension Plating efficiency. This term originally encompassed the terms
of fibroblast-like cells may secrete a glycosaminoglycan- attachment efficiency, cloning efficiency, and colony forming
collagen matrix and the result is a structure resembling fibrous efficiency; it is now better to use one or more of them in its place
connective tissue, which is, therefore, histiotypic. This term is because plating is not sufficiently descriptive. (See attachment
not meant to be used along with culture. Thus, a tissue culture efficiency, cloning efficiency, and colony forming efficiency.)

Glossary
Population density. The number of cells per unit area or
volume of a culture vessel, or the number of cells per unit
volume of medium in a suspension culture.
Population doubling level. The total number of population

doub-lings of a cell line or strain since its initiation in vitro. This
term is synonymous with cell generation time.
Population doubling time. The interval, calculated during

the logarithmic phase of growth in which cells double in
number; for example, 1.0 x 10 cells increase to 2.0 x 10 cells.
This term is not synonymous with cell generation time.
Primary culture. A culture started from cells, tissues, or

organs taken directly from organisms. A primary culture may
be regarded as such until it is successfully subcultured for the
first time. It then becomes a cell line.
Pseudodiploid. The condition in which the number

of chromosomes in a cell is diploid but, as a result of
chromosomal rearrangements, the karyotype is abnormal and
linkage relationships may be disrupted.
Saturation density. The maximum cell number attainable,

under specified culture conditions, in a culture vessel. This
term is usually expressed as the number of cells per square
centimeter in a monolayer culture or the number of cells per
cubic centimeter in a suspension culture.
Suspension culture. A type of culture which will grow and

can be maintained without attaching to a surface, such as
glass or plastic.
Transfection. The transfer, for the purpose of genomic

integration, of foreign DNA into cells in culture. The traditional
microbiological usage of this term implied that the DNA being
transferred was derived from a virus. The definition as stated
here describes the general transfer of DNA irrespective of its
source.
Undifferentiated. With animal cells, this is the state wherein

the cell in culture lacks the specialized structure and/or
function of the cell type in vivo.

References
References
1. Hayflick and Moorhead PS. Exp. Cell Res. 25: 585-621, 1961.
2. Rubin H. Mech. Aging Devel. 98: 1-35, 1997.
3. Wright WE and Shay JW. Nat. Biotechnol. 20: 682-688, 2002.
4. Capstick PB et al. Exp. Cell Res. 44: 119-128, 1966.
5. Osato et al. J. Immunology 124: 533-540, 1980.
6. McLimans WF. Chapter 5. In: Growth, Nutrition and Metabolism of Cells in Culture, Vol.1. Rothblat GH and
Cristofalo VJ, eds. New York: Academic Press; 1972.
7. Freshney RI. Chapter 8. In: Culture of Animal Cells, 5th ed. New York: Wiley-Liss; 2005.
8. Shipman C. Proc. Soc. Exp. Biol. Med. 130: 305, 1969.
9. People CA et al. In Vitro 18: 755, 1982.
10. Spierenberg GT et al. Cancer Res. 44: 2253, 1984.
11. Zigler JS et al. In Vitro 21: 282, 1985.
12. Karmiol S. Development of serum free media. In: Master JRW, ed. Animal Cell Culture, 3rd ed. Oxford: Oxford
University Press; 2000.
13. Jacoby WB and Pasten IH, eds. Chapter 7. In: Methods in Enzymology: Cell Culture, Vol. 58. New York: Academic
Press; 1979.
14. Bolin SR et al. J. Virol. Methods 48: 211, 1994.
15. Hyclone, Inc. Art to Science 15(1): 1-6, 1996.
16. Rudnicki MA and McBurney MW. Teratocarcinomas and Embryonic Stem Cells - A Practical Approach. Oxford:
IRL Press Ltd.; 1987: p. 75.
17. Weiss SA et al. Meth. Mol. Biol. 39: 65, 1995.
18. Gabridge MG. Vessels for Cell and Tissue Culture. In: Setting Up and Maintenance of Tissue and Cell Cultures.
Shannon: Elsevier Scientific Publishers; 1985: pp. 1-19.
19. Balin A.K et al. Atmospheric Stability in Cell Culture Vessels. In Vitro 12: 687-692, 1977.
20. Gey GO. Am. J. Cancer 17: 752-756, 1933.
21. Baust JM et al. Cell Preservation Technology 1: 17-31, 2002.
22. Baust JM et al. Cell Preservation Technology 1: 63-80, 2002.
23. Quality Control Methods for Cell Lines, 2nd edition. Rockville, MD: ATCC; 1992.
24. Freshney RI. Culture of Animal Cells, 5th ed. New York: Wiley-Liss; 2005.
25. Lincoln CK and Gabridge MG. Cell culture contamination: Sources, consequences, prevention and elimination.
In: Mather JP and Barnes D, eds. Animal Cell Culture Methods. San Diego: Academic Press; 1998: p. 49.
26. OBrien SJ. Science 98: 7656-7658, 2001.
27. Gartler SM. NCI Monograph 26: 167-195, 1967.
28. Master JR. et al. Proc. Natl. Acad. Sci. USA 98: 8012-8017, 2001.
29. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Biosafety in
Microbiological and Biomedical Laboratories, 5th ed. HHS Publication No. (CDC) 21-1112. Washington DC:
U.S. Government Printing Office; 2009. Available online at http://www.cdc.gov/biosafety/publications/
bmbl5/BMBL.pdf
30. Weiss RA. NCI Monograph 48: 183-189, 1978.
31. Schaeffer WI. In Vitro Cell. Dev. Biol. 26: 97-101, 1990.
32. Gazdar AF and Oie HB. Cancer Res. 46: 798-806 and 6011-6012, 1986.
33. Macy ML and Shannon JE. Preparation of medium ATCC-CRCM30. TCA Manual 3: 617-622, 1977.
34. Morton HJ. In Vitro 6: 89-108, 1970.
35. Eagle H. Science 122: 501-504, 1955.
36. Carney DN et al. Proc. Natl. Acad. Sci. USA 78:3185-3189, 1981.
37. Mitsuhashi J. Adv. Cell Culture 2: 133-196, 1982.
38. Waymouth C. J. Natl. Cancer Inst. 22: 1003-1017, 1959.

ATCC Media, Sera, and Reagents
ATCC Media product list
ATCC No. Product Name Volume
30-2604 AlphaMEM (Alpha Minimum Essential Medium) with nucleosides 500 mL
30-2605 AlphaMEM (Alpha Minimum Essential Medium) without nucleosides 500 mL
30-2002 Dulbeccos Modified Eagles Medium (DMEM) 500 mL
SCRR-2010 ES-DMEM 500 mL
30-2006 DMEM:F12 Medium (1:1 Ratio) 500 mL
30-2601 DMEM without phenol red 500 mL
30-2003 Eagles Minimum Essential Medium (EMEM) 500 mL
30-2004 F12K Medium 500 mL
46-X Hybri-Care Medium, Powder Prepares 1L
30-2005 Iscoves Modified Dulbeccos Medium (IMDM) 500 mL
30-2008 Leibovitzs L-15 Medium 500 mL
30-2007 McCoys 5A Medium, Modified 500 mL
30-2603 MCDB 131 Medium 500 mL
30-2001 RPMI-1640 Medium 500 mL
30-2602 RPMI without phenol red 500 mL
With the exception of Leibovitzs L-15 Medium, ATCC media are formulated* for use with 5% CO2. The amount of sodium bicarbonate in
each media ranges from 1.2 g/L to 2.2 g/L (1.5 g/L is the most common concentration).
* See the ATCC website for complete media formulations.
Animal Sera product list

30-2020 Fetal Bovine Serum 500 mL
30-2021 Fetal Bovine Serum 100 mL
SCRR-30-2020 Fetal Bovine Serum, ES Qualified* 500 mL
30-2030 Calf Bovine Serum 500 mL
30-2031 Calf Bovine Serum 100 mL
30-2040 Horse Serum 500 mL
30-2041 Horse Serum 100 mL
* Qualified for mouse and human embryonic stem cells.
Supplements and Antibiotics product list

30-2606 ITS Solution (Insulin, Transferrin, Selenious Acid) 10 mL
30-2214 L-Glutamine Solution 100 mL
30-2115 L-Alanyl-L-Glutamine Solution 100 mL

Supplements and Antibiotics product list continued

30-2116 MEM Non-Essential Amino Acid Solution* 100 mL
PCS-999-025 Gentamicin-Amphotericin B Solution 1.0 mL
PCS-999-002 Penicillin-Streptomycin-Amphotericin B Solution 1.0 mL
30-2300 Penicillin-Streptomycin Solution 100 mL
Buffers, Stains and Dissociation Reagents product list

30-2103 Non-Enzymatic Cell Dissociation Solution 100 mL
30-2104 Soybean Trypsin Inhibitor 20 mL
30-2101 0.25% Trypsin/0.53 mM EDTA Solution 100 mL
PCS-999-003 Trypsin-EDTA for Primary Cells* 100 mL
PCS-999-004 Trypsin Neutralizing Solution 100 mL
30-2200 Dulbeccos Phosphate Buffered Saline (DPBS)* 500 mL
30-2213 Hanks Balanced Salt Solution (HBSS)* 500 mL
SCRR-2201 Phosphate Buffered Saline (PBS)* 500 mL
30-2404 Erythrosin B Stain Solution 40 mL
PCS-999-001 Phenol Red 1.0 mL
30-2205 Water, Cell Culture Grade 500 mL
Cryopreservation Reagents product list

4-X Dimethylsulfoxide (DMSO) 5 x 5 mL
30-2600 Serum-Free Cell Freezing Medium 20 mL
Supplements and Antibiotics product list

PCS-999-027 0.1% Gelatin Solution 100 mL
Cell Proliferation Assays and Mycoplasma Detection

ATCC No. Product Name
30-1010K ATCC MTT Cell Proliferation Assay
30-1011K XTT Cell Proliferation Assay Kit
30-1012K Universal Mycoplasma Detection Kit

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Manassas, VA 20110
Tel 800.638.6597
703.365.2700
Fax 703.365.2750
Email [email protected]
Web www.atcc.org
Or contact your local distributor at

www.atcc.org/distributor
CB-0813-03
2014 American Type Culture Collection. The

ATCC trademark and trade name, any and all
ATCC catalog numbers and any other trademarks
listed in this publication are trademarks of
American Type Culture Collection unless
indicated otherwise. Nalgene and CryoMed
are trademarks of Thermo Fisher Scientific
Inc. StrataCooleris a registered trademark
of Agilent Technologies, Inc. PowerPlex is a
registered trademark of Promega Corporation.
GeneMapper is a registered trademark of Life ATCC CCL-2 HeLa
Technologies Corporation. Image courtesy of Thomas Deerinck, UCSD

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ATCC ANIMAL CELL CULTURE GUIDE

tips and techniques for continuous cell lines

Complete Growth Media............................................. 13 ATCC Media, Sera, and Reagents......................... 35

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Processing Flask Cultures

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Lag Phase Exponential Phase Stationary Phase

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Adapting to a New Medium or Serum

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1 2 hemocytometer with the cover slip.

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Subculturing Monolayer Cells

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Troubleshooting Monolayer Cell Subculturing

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Suspension Cell Subculturing

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Adapting a Monolayer Cell Line to Grow in Suspension

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Antibiotics and Antimycotics

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Description Growth area (cm) Recommended working Cell yield*

Cell culture dishes

Description Growth area (cm) Working volume (mL) Cell yield*

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Description Growth area (cm) Working volume (mL) Cell yield*

Surface Coatings and Feeder Cells

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ATCC No. Product Name Description

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Liquid Nitrogen Freezer Storage

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Recovery of Cryopreserved Cells

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Contamination and Biosafety

Check for Microbial Contamination

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Population doubling level. The total number of population

Population doubling time. The interval, calculated during

Primary culture. A culture started from cells, tissues, or

Pseudodiploid. The condition in which the number