Implen Nanophotometer User Manual V1.0.5

NanoPhotometer NP80/N60/N50/C40
User Manual
Version 1.0.5
NanoPhotometer NP80/N60/N50/C40 User Guide Version 1.0.5
Declaration of conformity for the NanoPhotometer (C40/N50/N60/NP80)
This is to certify that the Implen NanoPhotometer conforms to the requirements of the following
directives:
2014/35/EU Low Voltage Equipment Safety Directive
2004/108/EC EMC Directive
IEC 60529 Protection class IP20
2002/95/EC Restrictions on the use of certain Hazardous Substances

in Electrical and Electronic Equipment (ROHS)
2012/19/EU EC Directive on Waste Electrical and Electronic Equipment (WEEE)

2003/108/EC & 2008/34/EC. By ensuring this product is disposed of
correctly, you will help prevent potential negative consequences for the
environment and human health, which could otherwise be caused by
inappropriate waste handling of this product.
FCC 47 CFR Part15 §15.107 and §15.109
EN 301 489-1 V1.9.2 Radio and ancillary equipment for portable use (portable equipment); EUT
Operating frequency range: 2.4 – 2.4835 GHz
EN 301 489-17 V2.2.1 Electromagnetic compatibility and Radio Spectrum Matters (ERM)
IEC 62133 and UN38.3 Battery certification and transport test
Standards to which conformity is declared, where relent, are as follows:
IEC/EN 61010-1:2012 Safety requirements for electrical equipment for measurement, control and
laboratory use. General requirements.
EN61326-1:2013 Electromagnetic compatibility- generic emission standard electrical

equipment for measurement, control and laboratory use.
Signed:
Dr. Thomas Sahiri

Managing Director
Implen GmbH
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Contents
1. NANOPHOTOMETER AT A GLANCE ......................................................................... 6
NANOPHOTOMETER OVERVIEW ................................................................................................ 6
NANOPHOTOMETER NP80 ..................................................................................................................7
NANOPHOTOMETER N60 ....................................................................................................................8
NANOPHOTOMETER N50 ....................................................................................................................9
NANOPHOTOMETER C40 .................................................................................................................. 10
INSTRUMENT REAR PANEL (NP80/N60/N50/C40).............................................................................. 11
INSTRUMENT BOTTOM VIEW (NP80/N60/N50/C40) ............................................................................ 11
ACCESSORIES ....................................................................................................................... 12
STANDARD ACCESSORIES................................................................................................................. 12
OPTIONAL ACCESSORIES .................................................................................................................. 12
CONNECTIVITY....................................................................................................................... 14
NANOPHOTOMETER SPECIFICATIONS ...................................................................................... 15
2. GETTING STARTED.............................................................................................. 16
SPECTROPHOTOMETER INSTALLATION .................................................................................... 16
SOFTWARE INSTALLATION ...................................................................................................... 18
NPOS OVERVIEW............................................................................................................................. 18
REQUIREMENTS AND COMPATIBILITY ................................................................................................. 18
INSTALLING SOFTWARE ON COMPUTER .............................................................................................. 18
INSTALLING NANOPHOTOMETER APP ON TABLET OR SMART PHONE ................................................... 19
FIRST STEPS AND CONFIGURATION WIZARD ........................................................................................ 19
3. NANOPHOTOMETER BASICS ................................................................................ 20

APPLICATIONS OVERVIEW ...................................................................................................... 20
ICONS ................................................................................................................................... 22
BUTTONS .............................................................................................................................. 22
SIDE TAB BAR .................................................................................................................................. 23
DATA PROCESSING DIALOGS ............................................................................................................. 25
BASIC OPERATION ................................................................................................................. 27
NANOVOLUME MEASUREMENT BASICS (N50/N60/NP80) ................................................................... 27
CUVETTE MEASUREMENT BASICS (C40/NP80) .................................................................................. 28
SAMPLE HANDLING TIPS ................................................................................................................... 29
BATTERY OPERATION ............................................................................................................ 30
4. NANOPHOTOMETER APPLICATIONS ..................................................................... 32

NUCLEIC ACIDS .................................................................................................................. 32
METHOD OVERVIEW.......................................................................................................................... 32
3
MEASUREMENTS PROTOCOL ............................................................................................................. 32

CALCULATIONS ................................................................................................................................ 33
PROTEIN UV ...................................................................................................................... 38
METHOD OVERVIEW.......................................................................................................................... 38
CALCULATIONS ................................................................................................................................ 42
PROTEIN ASSAYS ............................................................................................................... 46
KINETICS .......................................................................................................................... 48
OD600 .......................................................................................................................... 49
METHOD OVERVIEW.......................................................................................................................... 49
CALCULATIONS ................................................................................................................................ 51
MORE APPS ................................................................................................................... 51
MORE APPS: WAVELENGTH ................................................................................................ 51
METHOD OVERVIEW.......................................................................................................................... 51
MEASUREMENT PROTOCOL ............................................................................................................... 52
CALCULATIONS ................................................................................................................................ 53
MORE APPS: WAVESCAN ................................................................................................... 53
METHOD OVERVIEW.......................................................................................................................... 53
CALCULATIONS ................................................................................................................................ 55
MORE APPS: ABSORBANCE RATIO ..................................................................................... 55
METHOD OVERVIEW.......................................................................................................................... 55
CALCULATIONS ................................................................................................................................ 57
MORE APPS: CONCENTRATION ........................................................................................... 57
METHOD OVERVIEW.......................................................................................................................... 57
CALCULATIONS ................................................................................................................................ 58
MORE APPS: STANDARD CURVE ........................................................................................ 59
METHOD OVERVIEW.......................................................................................................................... 59
CALCULATIONS ................................................................................................................................ 60
CUSTOM APPS ...................................................................................................................... 60
STORED RESULTS .............................................................................................................. 61
STORED METHODS ............................................................................................................. 62
5. PREFERENCES .................................................................................................... 63
GENERAL .............................................................................................................................. 63
4
DISPLAY .......................................................................................................................................... 63
ABOUT ............................................................................................................................................. 63
WIFI ACCESS POINT ......................................................................................................................... 63
ILLUMINATION SAMPLE WINDOW ....................................................................................................... 63
DYES 63
6. TROUBLESHOOTING ............................................................................................ 64
SELF-CALIBRATION TEST ........................................................................................................ 64
7. ASSISTANCE ....................................................................................................... 64
SUPPORT .............................................................................................................................. 65
REPORT PROBLEM ................................................................................................................ 65
SOFTWARE MAINTENANCE ..................................................................................................... 65
RESET ............................................................................................................................................. 65
SOFTWARE UPDATE .......................................................................................................................... 66
CONTACT IMPLEN .................................................................................................................. 66
8. MAINTENANCE .................................................................................................... 67
MAINTENANCE FREE TECHNOLOGY ......................................................................................... 67
REPLACEMENT PARTS ........................................................................................................... 67
CLEANING AND GENERAL CARE ............................................................................................. 68
9. WARRANTY......................................................................................................... 68
10. ALPHABETICAL APPENDIX ................................................................................... 69
5
1. NANOPHOTOMETER AT A GLANCE
NANOPHOTOMETER OVERVIEW
The Implen NanoPhotometer spectrophotometer is a mobile, simple to use UV/Visible instrument with
a CCD array detector with options ranging from nanovolume to standard cuvette and all-in-one
solutions. The N50, N60, and NP80 spectrophotometers measure sample volumes ranging from 0.3 -
2 µl. The NP80 model also has the capability to measure samples using a standard cuvette. The C40
is a mobile standard cuvette solution with the option to upgrade to accommodate nanovolume
measurements.
The NanoPhotometer runs on a Linux based operating system (NPOS) that is designed for the use of
pre-programmed and custom applications with a high degree of flexibility and processing power.
Sample Compression Technology™ provides easy sample handling which is independent of surface
tension. This technology squeezes the sample between two quartz surfaces allowing for unmatched
precision and accuracy without the need for dilutions. Combined with our True Path Technology™ the
system offers lifetime accuracy and precision without the need for maintenance or recalibration.
Note: It is recommended to use a properly calibrated pipette with high quality tips to ensure delivery
of appropriate sample volumes for nanovolume sample applications.
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N ANOPHOTOMETER NP80
Item Number Touchscreen Battery Pack

NP80 - -
NP80-Touch + -
NP80-Mobile + +
7
N ANOPHOTOMETER N60

N60 - -
N60-Touch + -
N60-Mobile + +
8
N ANOPHOTOMETER N50

N50 - -
N50-Touch + -
9
N ANOPHOTOMETER C40

C40 - -
C40-Touch + -
C40-Mobile + +
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INSTRUMENT REAR PANEL (NP80/N60/N50/C40)
INSTRUMENT BOTTOM VIEW (NP80/N60/N50/C40)
Model name, device serial number and FCC ID are located on the identification plate on the bottom of
the instrument.
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ACCESSORIES
STANDARD ACCESSORIES
 Connecting Cable
The USB cable provided makes it possible to connect the NanoPhotometer to a computer to control
the instrument from the computer (please see Software Installation).
 NanoPhotometer Power Adapter
Use the power adapter to plug in the NanoPhotometer for use and/or charge the NanoPhotometer
battery (touch and mobile models with optional integrated battery).
Note: Use only the power adapter, supplied with your instrument or a replacement part from the
manufacturer or your supplier.
 Dust Cover
OPTIONAL ACCESSORIES
 Didymium Glass Filter (C40/NP80)
The certified didymium glass filter is used as a control of

wavelength and photometric accuracy for the NanoPhotometer
cuvette applications.
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 Submicroliter Cell (C40 only)

The submicroliter cell provides the option of upgrading the
NanoPhotometer C40 to a device that handels nanovolume samples as
well as cuvette samples. The sample volume range of the submicroliter
cell ranges from a minimum of 0.3 µl to 5.0 µl with the path length
options including: 0.04 mm, 0.1 mm, 0.2 mm, 1 mm and 2 mm which
correspond to virtual dilution factors of 1:250, 1:100, 1:50, 1:10, and 1:5
respectively.
 DiluCell (C40/NP80 only)

The DiluCell is a disposable cuvette with shortened path length for virtual
dilution of cuvette based samples. Due to the reduced path length the
DiluCell provides an automatic dilution without the need of a physical
dilution of higher concentration samples. There are two different sizes of
DiluCells available DC 10 and DC 20 which allow an automatic 1/10 and
1/20 dilution of the sample respectively. Bypassing manual sample
dilutions reduces dilution errors and cross contamination making DiluCell
ideal for GLP. Combined with small sample volume requirements and
bubble free filling, the Dilucell allows for convenient spectrophotometric
analysis from 340 - 950 nm.
 Field Kit
Implen aluminium roller case for safe transportation, designed to fit in most airplane overhead bins;
special compartments for all necessary accessories, cleaning tools and samples.
Note: Delivered w/o NanoPhotometer and accessories

Note: Only operate the NanoPhotometer in the roller case when cover is open. Ensure that air
circulation is possible. Switch the NanoPhotometer always off for transportation.
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CONNECTIVITY
 WiFi
The NanoPhotometer has a WiFi hotspot capability. This provides the option to control the
NanoPhotometer by other WiFi devices like smart phones or tablets.
SSID: NanoPhotometer serial number; password: Implenuser
 USB A
There is a USB A port on the front and rear panel of the NanoPhotometer which is compatible with
standard portable USB storage devices for direct data transfer in a variety of formats including Excel.
It is also possible to connect a mouse or keyboard directly to the NanoPhotometer.
 USB B
There is a USB B port located on the rear panel of the instrument which is compatible with the USB
cord provided to connect the NanoPhotometer to a computer. This USB connection can be used to
control the NanoPhotometer via a computer.
 LAN
There is an Ethernet (LAN) connection port on the rear panel of the instrument which enables the
NanoPhotometer to connect with computers within close proximity.. This Ethernet connection can be
used to transfer data from the NanoPhotometer to a computer. To access the directory of the
NanoPhotometer via LAN enter the serial number/IP of the NanoPhotometer in the Windows-
Explorer/Mac OS X Finder and confirm with the Enter key.
Note: The maximal LAN cable length is 10 meters. Bit rate is 1 Gbit/s.
 HDMI
There is an HDMI port located on the rear panel of the NanoPhotometer which is compatible with
HDMI 1.4 (or better) cables to connect the NanoPhotometer to HDMI compatible monitors.
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NANOPHOTOMETER SPECIFICATIONS
NanoVolume Performance
Detection Range dsDNA 1 ng/µl to 16,500 ng/µl (N50: 5 ng/µl to 7,500 ng/µl)
Detection Range BSA 0.03 mg/ml to 478 mg/ml (N50: 0.15 mg/ml to 217 mg/ml)
Minimum Sample Size 0.3 µl
Photometric Range (10 mm equivalent) 0.02 - 330 A (N50: 0.1 – 150A)
Path length 0.67 and 0.07 mm
dilution factor 15 and 140
Vortexer 2,800 rpm; tube size up to 2.0 ml
Cuvette Performance
Detection Range dsDNA 0.1 ng / µl to 130 ng / µl
Detection Range BSA 0.003 mg / ml to 3.7 mg / ml
Photometric Range 0 - 2.6 A
Center Height (Z-Height) 8.5 mm
Cell Types outside dimension 12.5 x 12.5 mm
Heating 37°C ± 0.5°C
Optical Specifications
Wavelength Scan Range 200 – 900 nm (N50: 200 - 650 nm)
Time for Full Scan Range 3.5 – 6.0 seconds
Wavelength Reproducibility ± 0.2 nm (N50: ± 1nm)
Wavelength Accuracy ± 0.75 nm (N50: 1.5 nm)
Bandwidth 1.8 nm (N50: 5 nm)
Stray Light < 0.5% at 240 nm using NaI (N50: < 2%) and
< 1% at 280 nm using Acetone (N50: < 2%)
Absorbance Reproducibility < 0.002 A (0.67 mm path) @ 260 nm
(N50: < 0.004 A (0.67 mm path) @ 260 nm)
Absorbance Accuracy < 1.75 % @ 0.7 A (0.67 mm path) @ 260 nm of the reading
Zero Stability ±0.003 A/hour after 20 min warm up @ 260 nm
Noise 0.002 A rms at 0 A @ 260 nm; 0.002 A (pk to pk) at 0 A @ 260 nm
Optical Arrangement 1 x 3648 CCD Array (N50: 1 x 1024 CCD Array)
Lamp Xenon flash lamp
9
Lifetime 10 flashes, up to 10 years
Processing Power and Compatibility

Operating System Linux based OS
Onboard Processor Quad Core 1 GHz
Internal Storage 8 GB
Control Options Onboard with built-in touchscreen, computer, smart phone and tablet
Software Compatibility Windows 7 (32 and 64 bit), Windows 8 (32 and 64 bit), OS X, iOS and
Android
Min. Requirement Smart 4 inch screen;
phone/Tablet Apple: iPad 2, iPhone5 and iOS 6
Android version 2.2, Quadcore 1.2 GHz with 1 GB RAM
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General Specifications
Size 200 mm x 200 mm x 140 mm
Weight 3.8 – 5.2 kg depending on configuration
Operating Voltage 90-250 V, 50/60 Hz, 60 W (90 W with battery pack), 18/19 VDC
Display 1024 x 600 pixels; touchscreen glove compatible
Certifications CE, IEC/EN 61010-1:2012 and EN 61326-1:2013
Battery Pack optional rechargeable lithium ion battery; 95Wh, 6,6Ah;
Operation time: up to 8 h; min. charging cycles: 800
Battery Certification IEC 62133 and UN38.3 transport test
In- and Output Ports 2x USB A, USB B, HDMI, Ethernet, WLAN
Additional Data Input Mouse and keyboard options
Security Slot for Kensington lock
Features and specifications are subject to change without notice.
US Patents 20080204755 and 20080106742
Windows is a trademark of Microsoft. Mac OS & iOS are trademarks of Apple. Android OS is a trademark of Google. Linux is a trademark of
Linus Torvalds.
2. GETTING STARTED
SPECTROPHOTOMETER INSTALLATION
 Safety Information
Before commencing installation, please take time to familiarize yourself with warning labels and
symbols on your instrument and their meaning. These are to inform you where potential danger exists
or particular caution is required.
direct current
Do not open the instrument as this can expose the operator to electrical power, UV light and delicate
fiber optics.
Do not use damaged power cords, accessories, and other peripherals with your NanoPhotometer.
Do not expose the NanoPhotometer to strong magnetic or electrical fields.
Do not leave your NanoPhotometer on your lap or near any part of your body to prevent discomfort or
injury from heat exposure.
Do not place objects on top of your NanoPhotometer.
The NanoPhotometer with battery pack (mobile version) has to be switched off during transportation.
The on/off button has to be protected from turning on itself caused by shock or vibration.
The symbol on the product, or on the documents accompanying the product, indicates that this
appliance may not be treated as household waste. Instead it shall be handed over to the applicable
collection point for the recycling of electrical and electronic equipment. Disposal must be carried out
in accordance with local environmental regulations for waste disposal.
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 Unpacking and Positioning

Check the contents of the package against the delivery note. If any shortages are discovered, inform
your supplier immediately.
Inspect the instrument for any signs of damage caused in transit. If any damage is discovered, inform
your supplier immediately.
Ensure your proposed installation site conforms to the environmental conditions for safe operation:
indoor use or dry environment.
Note: Do not expose your NanoPhotometer near liquids, rain, moisture or dusty environments.
Temperature range 10 - 40 °C; If the cuvette heating is used the range is 10 - 30°C.
If the instrument is subjected to extreme temperature changes, it may be necessary to allow the
instrument to equilibrate and to turn the instrument off and then on again once thermal equilibrium
has been established (~2 - 3 hours).
Maximum relative humidity (non-condensing) of 80% and up to 31°C decreasing linearly to 50% at
40°C.
The instrument must be placed on a stable, level surface that can support 4 - 5 kg and so that air can
circulate freely around the instrument. Ensure while powered on that no materials reduce air
circulation.
The equipment should be positioned such that in the event of an emergency the main plug can be
easily located and removed.
Carry the instrument always by holding the main corpus of the instrument and not e.g. on the optional
attached display or NanoVolume pedestal.
The equipment must be connected to power with the 60W power supply/cord supplied by Implen
(90W with battery pack). It can be used on 90 - 250 V, 50 - 60 Hz power supply system.
For Mobile models please load the battery pack at least for 3 hours prior to the first use.
Turn the instrument on using the power button on the rear panel after it has been plugged in. The
instrument will perform a series of self-diagnostic checks.
Please read the complete user manual prior to use.
Please contact original supplier immediately if technical or sample handling difficulties are
experienced.
Note: If this equipment is used in a manner not specified or in environmental condition not suitable for
safe operation, the protection provided by the equipment may be impaired and the instrument
warranty voided.
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SOFTWARE INSTALLATION
NPOS OVERVIEW
NPOS is a Linux based operating system designed for the NanoPhotometer.
NPOS can store data either to a common directory or be configured to save to independent
directories according to file format and/or instrument.
NPOS can save data in an Implen .IDS format or as an Excel format file.
Note: Please do not connect the instrument to a computer until the NanoPhotometer NPOS software
is installed on the computer.
REQUIREMENTS AND COMPATIBILITY

The NPOS user interface is designed that all features can be operated by using a touchscreen. If the
software is installed on a computer without touchscreen, the user interface can be operated by using
a keyboard and a mouse. Before starting the installation process ensure the device is compatible with
the requirements for installation.
Compatible Control Devices
Computer:
PC: Windows 7 / Windows 8 (32 bit or 64 bit)
Mac: OS X
Tablets:
iPad 2: iOS6
Android (Quadcore 1.2 GHz with 1 GB RAM): Android version 2.2
Smart phones:
iPhone 5: iOS6
Android (Quadcore 1.2 GHz with 1 GB RAM): Android version 2.2
Windows is a trademark of Microsoft. Mac OS & iOS are trademarks of Apple. Android OS is a trademark of Google. Linux is a trademark of
Linus Torvalds.
Note: There are two user interfaces of the software available; one for built-in touchscreen, computer
and tablets and one for smart phones.
INSTALLING SOFTWARE ON COMPUTER

The NanoPhotometer software can be installed on compatible PC and Mac computer systems.
Various operating systems and PC hardware may cause the set-up procedure to differ from that
described here. This process is given as guidance only; it may need adaptation for other systems. To
prevent loss of data it is important to ensure that connections are stable and not lost during data
transmissions and ensure that the system has enough time to save transferred sample data.
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1. To install the NanoPhotometer software the installer should be logged with full administration
rights. If you have insufficient privileges, installation may fail. If in doubt consult your PC
administrator.
2. Connect the instrument to the computer using the USB cable provided
Note: The Windows and Mac installation file is provided on the Implen USB flash drive which is
included in the NanoPhotometer delivery and are available for free download in the download section
of the Implen webpage.
Note: If there is Avira installed on your computer, it is recommended to switch of the browser safety.
This may interfere with the NPOS running on your computer.
INSTALLING NANOPHOTOMETER APP ON TABLET OR SMART PHONE

The NanoPhotometer App can be installed as an application on tablets and smart phones with
compatible Android and iOS operating systems. The NanoPhotometer App is available for free
download in the app store (Apple Store and Google Store).
1. Download and install the NanoPhotometer App from the app store
2. Use the WiFi to connect the NanoPhotometer to the tablet or smart phone.
SSID: Serial number, password: implenuser
3. Open the NanoPhotometer App
4. When connected via WiFi the NanoPhotometer will recognize the tablet as a remote control
device and measurements can be initiated from the tablet or smart phone
5. Measurement results will be shown to the tablet or smart phone once taken
Note: In order to install the NanoPhotometer App on a tablet or smart phone, the device must have
an established internet connection to access the app store for app download.
FIRST STEPS AND CONFIGURATION WIZARD

Starting the Implen NPOS the first time an Implen configuration wizard is shown. Please confirm the
End User License Agreement (EULA) and select the country in which the NanoPhotometer is used
and confirm.
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3. NANOPHOTOMETER BASICS
The NanoPhotometer product line offers a complete solution for Nanovolume (NP80/N60/N50/C40)
and standard cuvette volume (C40/NP80) applications. With the NanoPhotometer nanovolume
applications the sample volume ranges from a minimum of 0.3 μl to a maximum sample volume of 2.0
µl. Standard cuvette applications can be performed with 10 mm, 5mm, 2 mm and 1 mm path length
quartz, glass, or plastic cuvettes with a center height of 8.5 mm.
APPLICATIONS OVERVIEW
The NanoPhotometer comes with pre-programmed applications as well as the ability to create custom
applications. To select a method click/tap on the corresponding icon and the method will open
immediately.
Method Icons Description
Nucleic Acids Concentration, purity, and dye incorporation for DNA, RNA,
Oligo, and other nucleic acids
Protein UV Protein UV determination at 280 nm (or in a range of 200 -

330 nm), purity and dye incorporation
Kinetics Time vs. Absorbance readings
Protein Assays* BCA (562 nm), Bradford (595 nm), Lowry (750 nm), and Biuret
Assays (546 nm)
OD600* Measures cell density at 600 nm (or in a range of 200 – 900

nm)
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Stored Methods Collection of stored custom methods
Stored Results Archive of stored results
More Apps Additional applications found on a secondary method screen
Define one or multiple wavelength between

Wavelength 200 – 950 nm (N50: 200 – 650 nm) for absorbance
measurements
Define desired full scan range anywhere between

Wavescan
200 - 950 nm (N50: 200 - 650 nm)
Define extinction coefficient for automatic

Concentration
concentration calculations
Absorbance/ Define two wavelengths for a calculated absorbance/

Ratio ratio
Standard Curve Create a standard curve at a defined wavelength
Optional custom applications for personalized

Custom Apps
methods tailored to individual spectroscopy needs
Note: *For Protein Assays and OD600 applications the cuvette mode is recommended.
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ICONS
Icon Name Action
WiFi Hotspot WiFi hotsopt enabeld; can be disabled in preferences
Assistance Opens the assistance page
Shows the actual battery status (only shown with optional battery
Battery Status
pack)
Preferences Opens the preferences page
Returns to the home screen with application icons for method

Home Screen
selection.
Leave Method Returns to the previous application selection
Back Returns to the previous page (smart phone only)
Next/Confirm Confirms parameter and opens the next screen (smart phone only)
Delete Deletes added functions in parameter; empties input windows
Delete Data Opens a delete dialog pop up
Email Data Opens an email dialog pop up (computer and tablet versions only)
Save Data Opens a save dialog pop up
Add Folder Adds a new folder to the directory
Opens a dialog pop up with several action options including delete,

Manage Data rename or import folders/files/data as well as copying or move
folders/files/data to defined directories
Opens a dialog pop up with the possibility to store the actual method
Store Method
parameter to a custom method
Full Scale Restores graph to original size without zoom
Cancel Returns to the previous screen without implementing any changes
BUTTONS
Prior to any sample measurement at the start of a new method a blank
measurement of either water or the buffer of the samples is required to give
the NanoPhotometer a reference of what zero should be. It is
recommended to re-apply the blank and measure it as a sample to ensure
the graph of the blank spectra is a flat line.
Note: Use always a minimum of 1 µl for any blank measurement.
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To initiate the spectral scan of the sample press the sample button. The
data will be temporarily stored until the method is exited at this time the
user needs to define if the samples should be saved or deleted.
The Change to Cuvette button (NP80) is located at the button of the

parameter window. The change to cuvette/nanovolume button toggles
between nanovolume and cuvette applications. Selecting the Change to
Cuvette button activates the cuvette compartment (opens the sliding cover
and switches the red arrow LED on). Only cuvette measurements are
possible when this mode is selected. Selecting the Change to Cuvette
button while it is activated will deactivates the cuvette compartment (closes
the sliding cover and switches the LED off) and only nanovolume
measurements are possible.
Note: Please make sure that the nanovolume arm is closed during cuvette measurements.
The Change to NanoVolume button (C40) is only shown when submicroliter

cell applications are enabled. The Change to NanoVolume/Cuvette button
toggles between cuvette and submicroliter cell applications. With the
NanoVolume submicroliter application the parameter of each method show
a dropdown for lid selection (Lid 5, 10, 50, 100 and 250). Choose the
correct lid and the results are automatically calculated considering the
virtual dilution.
SIDE TAB BAR

On the left side of the measurement screen there is a vertical tab bar that contains four tabs
including: parameters, data, graph, and table. The different tabs allow organizing the
measurement screen. It is possible to show or hide the different areas on the screen. Default
screen for computer show all areas, for the built-in screen and tablet version the table is hidden.
Parameter
Results
Graph
Table
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Note: There is no tab bar available for smart phone versions. The parameters, results and
graph screens are shown full screen. Parameters need to be confirmed ( ) to get to the
measurement screen. It is possible to toggle between the results and graph area by sliding left
and right. There is no table area available on smart phones.
 Parameter area
In the parameter area it is possible to define all necessary parameters for a measurement as
well as turn on cuvette mode and initiate cuvette heating. The default measurement screen
includes the parameter area as open. It is automatically hidden when starting either a blank or
sample measurement by clicking on the Blank or Sample button. It is also possible to hide the
parameter area by tapping the parameter tab in the vertical side tab bar.
 Results area
The results area shows the method specific results of the latest measurement including
concentration, absorbances, and relevant ratios from the last sample measured. It is also
possible to change the units of the calculated concentrations in the results area with a drop-
down selection menu.
Note: Selection of one or more than one line is selected in the table no data are shown in the
result view.
 Table area
The table area collects defined results for all samples completed during the active method. The
first column of the table indicates whether the measurement is saved ( ) or not saved (blank
field).
 Graph area
The graph area shows a chart with the graph of the actual measurement or the selected line(s)
in the table. There is an overlay toggle switch on the left bottom of the graph area. If the overlay
option is enabled the graphs of the measurements will be automatically overlaid. To change the
overlaid graphs select/deselect the samples in the table.
Note: It is only possible to overlay up to 30 graphs in a chart. If more than 30 data are selected
a message will appear that says “Too many data selected. Up to 30 data can be overlaid.”
Please select the desired data to be displayed on the graph.
Note: The overlay button is not available on the NanoPhotometer and smart phones, only on
tablets and computer versions.
It is possible to zoom in and out any area of the diagram (x- and y-axis). Undo the zoom by
clicking the full scale icon ( ).
Note: Maximum zoom is 20 nm for the x-axis and 0.01A for the y-axis.
24
As legend option the sample name in the table is colored in the same color as the graph in the
chart.
Clicking on the graph opens a pop up which shows the sample name, wavelength and
absorbance of the selected wavelength. It is possible to show results of further graphs by
changing the sample in the sample name drop-down.
D ATA PROCESSING DIALOGS

 Save
Selecting the save data icon ( ) opens a full screen overlay dialog window with various save
options.
Save selected
This option saves the current selection of data of the table. If the save selected toggle switch is
green the save all toggle switch will automatically be deactivated.
Save all
The save all button (default setting) allows the user to save all of the data from the current
method. If the save all toggle switch is green the save selected toggle switch will automatically
be deactivated.
Note: On the smart phone app there is no save selected/save all toggle switch available;
instead in this case the entire measurement session is saved.
Save as
The save as button allows the user to specify which type of file to save the data as. The options
of file types include: Excel and Implen Document Source (IDS), which can be saved to
NanoPhotometer, Control Device and on USB flash drive.
Note: Control Device is only available on smart phones and tablets.
Implen Document Source File
25
Implen has a custom file format referred to as being an Implen Document Source (IDS) file. This
is a hardcopy file to which no changes can be made. This file type contains all information
including raw data, results, values, and parameters. The saved file shows only the selected
information at the time the file was saved. IDS files can only be opened with the Implen
software. The data are opened in the measurement.
Excel File
Data from the measurements can also be saved in an Excel file format. This file format is
compatible with Microsoft Excel software versions 2007/2010/2013 and can be edited. This file
type contains all information including raw data, results, and parameters. The saved file
contains only the selected information at the time the file was saved.
Storage
Selection option to choose the device the data should be saved to. The options include:
NanoPhotometer, USB flash drive (if connected) and Control Device (for smart phones and
tablets only). If Control Device is selected the data will be transferred to the device that is
currently connected with the NanoPhotometer.
 Delete
Selecting the delete icon ( ) opens a full screen overlay dialog window with delete options.
Delete selected
This option deletes the current selection of data in the table. If the delete selected toggle switch
is green the delete all toggle switch will automatically be deactivated.
Delete all
The delete all button allows the user to delete all of the data from the current method. If the save
all toggle switch is green the save selected toggle switch will automatically be deactivated.
Once the delete button is selected a message will appear asking “Do you want to delete
all/selected files?” selecting cancel will return to the delete menu screen and selecting delete
will delete the selected data.
26
Note: The delete function is not available for the software version designed for smart phones.
BASIC OPERATION
The NanoPhotometer product line offers a complete solution for nanovolume
(N50/N60/NP80/C40) and standard volume (C40/NP80) applications. With the NanoPhotometer
nanovolume applications the sample volume ranges from 0.3 µl to a maximum sample volume
of 2.0 µl. Standard Cuvette applications can be performed with 10 mm, 5 mm, 2 mm and 1 mm
path length quartz, glass, or plastic cuvettes with a center height of 8.5 cm.
Note: NanoVolume application in the NanoPhotometer C40 is only available with the optional
accessory “submicroliter cell” from Implen.
N ANOVOLUME M EASUREMENT B ASICS (N50/N60/NP80)

1. Select a method depending on your sample and set the parameter for the measurement.
2. Ensure that the sample window and the mirror in the sample arm are clean.
3. Use the integrated vortexer (N60 and NP80 only) to mix your sample to achieve an
homogenous sample
4. Raise the sample arm and pipette the appropriate amount of sample onto the illuminated
sample window. The illumination turns automatically off, lowering the arm.
Note: Do not overfill the well.

Note: Save, low energy red light (LED)
5. Lower the sample arm and initiate a blank measurement with the blank button
6. Clean the measurement window and mirror on the sample arm with a slightly wet lint-free
tissue. Use water, 70% ethanol or isopropanol.
27
Note: Make sure that the metal contact face (around the measurement window and the
mirror) is clean.
Note: Do not use aggressive solvents such as strong acids or bases or organic solvents at
any time. If unsure please contact [email protected] for detailed information about your
specific reagent/solvent.
7. Raise the sample arm and pipette the appropriate amount of sample solution onto the
illuminated sample window (1 - 2 µl for automatic path length change or 0.3 µl for dsDNA >
120 ng/µl / BSA > 12.6 mg/ml). Upon completion of measurement raise sample arm, clean
the surfaces and apply the next sample.
Note: The sample window must be clean and residual fluff from any cleaning wipe must be
removed for optimum performance.
CUVETTE M EASUREMENT B ASICS (C40/NP80)

The NanoPhotometer (NP80 and C40 only) is compatible with standard cuvettes having an 8.5
mm center height. The light path is indicated with a red status LED arrow for the NP80 model
and with two white arrows for the C40 model.
Note: For the NP80 the cuvette compartment needs to be activated by the “Change to Cuvette”
button in the parameter area. Once the cuvette option is activated the sample compartment
door will be opened automatically and a red arrow above the cuvette compartment will appear.
The arrow indicates the light path.
1. Open the cuvette cover by clicking the “Change to Cuvette” button below the parameter
area (NP80).
28
2. Add a blank solution to the cuvette and ensure that the filling volume is sufficient to allow
light path to pass through the solution.
3. Insert cuvette into the cell holder.
4. Initiate a blank measurement with the blank button. Upon completion of measurement
remove the cuvette.
5. Add sample to cuvette and ensure that the sample volume is sufficient to allow light to pass
through the sample.
6. Initiate a sample measurement with the sample button. Upon completion of measurement
remove the cuvette
7. Apply further samples.
SAMPLE H ANDLING TIPS

 Nanovolume Methods
 The NanoPhotometer includes an integrated vortexer (N60/NP80 only) to assure sample

homogeneity. It is recommended to vortex every sample right before the measurement.
 The sample window is illuminated with a low energy red light to assist with accurate sample
application. The red light is switched off once the sample arm is closed. It is possible to
disable the illumination feature in preferences of the NPOS.
 The minimum volume that can be used for nanovolume samples is 0.3 µl (starting for
dsDNA > 120 ng/µl and BSA > 12.6 mg/ml). For automatic path length setting at least 1µl is
needed.
 The maximum volume that can be used for nanovolume samples is 2.0 µl.
 The sample can be fully recovered after measurement with a pipette if desired.
Note: Minimal cross contamination cannot be avoided on a molecular level.
 Proper cleaning is important to ensure accurate measurements. In most cases a dry lint-free
laboratory wipe is sufficient to clean the sample quartz surfaces. In the case of highly
concentrated samples or certain proteins, the recommended procedure for cleaning is to
use a slightly wet lint-free laboratory wipe (with water or 70% EtOH depending on sample
type) to thoroughly clean the sample surface.
 It is mandatory that the metal contact face around the measurement window and the mirror
is clean.
 Cuvette Methods
29
 The cuvette holder (NP80/C40 only) is compatible with standard 10 mm path length quartz,
glass and plastic cuvettes with an optical height of 8.5 mm.
 It is also possible to use cuvettes with 5 mm, 2 mm or 1 mm path lengths, but there may be
an adapter necessary. Please ask your cuvette supplier for suitable adapter.
 The minimum volume for accurate measurements depends on the cuvette type used; it is
necessary for the light path to pass through the sample for accurate measurements.
Note: The cuvette holder is not removable. Do not pour any cleaning solution into the cuvette
holder as larger amounts of liquids can get into the instrument and cause damage.
 Solvent Compatibility (N50/N60/NP80)

Most solvents typically used in life science laboratories are compatible with the
NanoPhotometer nanovolume sample surfaces. The following solvents are compatible for use
with the NanoPhotometer models N50, N60, and NP80 at room temperature:
 Acetone (≤ 5%)  Methylenchlorid

 Acetonitrile  MOPS
 Benzene  Phenol (≤ 1%)
 Butanol
 N-propanol
 Carbon tetrachloride
 Toluene
 Chloroform
 Phosphate containing buffers
 Ether
 PBS (pH 4-10)
 HEPES
 Citrate
 Hexane
 Borate
 Isopropanol
 Chloride salts
 MES
 Acids > pH 2
 Methanol
 Bases < pH 10
Note: Highly concentrated acids and bases are not recommended. It is recommended to wipe
the sample surface with a lint-free laboratory wipe immediately upon completion of each
measurement. For more information about compatibility of specific solvents not listed above,
please contact the Implen support team ([email protected]) to check the compatibility.
BATTERY OPERATION
The optional battery operation is only available for NP80-Touch, N60-Touch and C40-Touch
models. A full battery pack can be operated for approximately 8 hours within normal usage, i.e.
30
20-30 measurements per hour. When the battery gets low there will be a first warning message
“Battery low” and a bleep is sounded. At this status it is possible to use the instrument under
standard conditions at least for 1 hour. It is recommended to charge the battery at this status. If
the battery is not charged there will be a second warning message when the battery is empty
and several beep sounds before the instrument is automatically shutting down within 10 to 15
seconds.
Note: Unsaved data can be found in the autosave folder in Stored Methods. If the
NanoPhotometer is shutting down during a measurement process the data of this measurement
are lost.
The battery pack is designed for 800 full charging cycles. Afterwards the capacity and operation
time of the battery may vary. A fully charged battery pack will self-discharge (switched off
NanoPhotometer) over a time of 10 – 14 days. After this time recharging of the battery pack is
necessary.
31
4. NANOPHOTOMETER APPLICATIONS
The NanoPhotometer comes with pre-programmed applications as well as the ability to create
custom applications. Any application method can be selected by tapping the icon once or
clicking on the icon (computer based software).
Note: To select a method select the corresponding icon. Selection of nanovolume or cuvette
mode is within each method possible. The “Change to Cuvette” or “Change to NanoVolume”
button is located at the bottom of the parameter area.
NUCLEIC ACIDS
M ETHOD OVERVIEW
Nucleic acids in solution absorb light with a peak in the ultraviolet region of 260 nm. For
determination of nucleic acid concentration in solution the absorbance at wavelength 260 nm is
used along with the Beer-Lambert law. In addition to calculating concentrations of nucleic acids,
absorbance measurements are also useful for estimating purity of nucleic acids by calculating
the 260:280 nm and 260:230 nm ratios. Further, it is possible to determine the degree of
labeling of nucleic acids with probes including fluorescent dyes.
M EASUREMENTS PROTOCOL
1. Select the Nucleic Acids icon on the home screen.
To change between NanoVolume and cuvette application (NP80/C40 only)
use the Change to Cuvette/NanoVolume button below the parameter area.
2. Select the nucleic acid type in the drop-down of the parameter area.
Options are: dsDNA, ssDNA, RNA miRNA, miRNA Sequence, Oligo, Oligo
Sequence and Custom (see Table 1).
• The miRNA sequence and Oligo sequence options allow having the
sequence entered and the extinction coefficient will be automatically
calculated.
• Custom is set to 50 as a default and allows the extinction coefficient to be
manually entered from the range of 15 - 150 up to three decimal points.
3. For NanoVolume application:

Select the volume of sample to be applied.
Note: 1 - 2 µl (default): automatic path length change; 0.3 µl measures only
the 0.07 mm path length (for samples with concentrations >120 ng/µl
dsDNA)
32
For cuvette application:

Select the path length depending on the used cuvette.
Options are: 1 mm, 2 mm, 5 mm and 10 mm
4. If it is desired to heat the sample to 37°C use the toggle switch to turn on
cell holder heater. When the cuvette holder has 37°C the color changes to
green.
Note: Only available for cuvette applications (NP80 and C40).
5. The background correction is enabled as the default. It is possible to disable

the background correction with the toggle switch.
6. If a dye labeled sample is used please add a dye by tapping on the Add Dye
Label option and select a dye from the drop-down list. There is also an
option for dye correction which can be en-/disabled with a toggle switch.
Added Dyes can be deleted by tapping on the delete icon ( ).
Note: If the used dye is not available in the drop-down list, please go to
preferences and add a custom dye to the dye list.
7. Option to set/calculate a dilution factor for manual diluted samples.
8. Apply the blank ddH20 or buffer to the illuminated sample window for the
reference measurement and select blank to initiate the reading.
Note: The illumination of the sample window can be switched off in the
preferences.
9. Use a lint-free laboratory wipe to clean both the sample window and mirror
prior to applying the next sample.
Note: It could be helpful to apply the blank a second time and read it as a
sample to ensure a proper blank.
10. Apply sample to the sample window and press the sample button to initiate
the measurement.
C ALCULATIONS
 Nucleic Acid Concentration
To determine the concentration of nucleic acids in solution, the absorbance as measured at the
wavelength of 260 nm is used. The function describing the relationship between concentration
and absorbance is a modification of the Beer-Lambert law equation. The concentration of the
33
nucleic acid samples can be calculated with or without background correction depending on if
the background correction is turned on for the measurements.
Without background correction:
C = A260 * εnuc * Đ
With background correction:
C = (A260 - A320 ) * εnuc * Đ
C Concentration in ng/µl
A260 Absorbance at 260 nm (10 mm path)
Đ Manual dilution factor
εnuc Extinction coefficient/nucleic acid factor in ng*cm/µl
Table 1. Nucleic acids extinction coefficients (εnuc )
Type εnuc
dsDNA 50 ng*cm/µl
ssDNA 37 ng*cm/µl
RNA 40 ng*cm/µl
miRNA 33 ng*cm/µl
Oligo 33 ng*cm/µl
miRNA Seq. calculated via extinction coefficient of constituent nucleotides entered
Oligo Seq. calculated via extinction coefficient of constituent nucleotides entered
Custom Option to enter any factor between 15 and 150 ng*cm/µl
 Dye-labeled Nucleic Acid Concentration

For dye-labeled nucleic acids, the concentration of the nucleic acid is calculated using a
modified form of the Beer-Lambert equation. For these calculations, the instrument considers
the absorption maximum of the dye and a certain dye-specific correction factor at 260 nm (see
Table 2). The concentration of a dye-labeled nucleic acid is calculated with or without
background/dye correction as follows:
With background and with dye correction:
C = [(A260 − A320 ) − (cfdye * (Amax,dye − A320 ))] * εnuc * Đ
With background and without dye correction:
C = (A260 − A320 ) * εnuc * Đ
34
Without background and with dye correction:
C = [A260 − cfdye * Amax,dye ] * εnuc * Đ
Without background and without dye correction:
C = A260 * εnuc * Đ
Amax,dye Absorbance value at the absorbance maximum of the dye (10 mm path)
cfdye Dye-dependent correction factor at 260 nm
 Dye Concentration
For dye-labeled nucleic acids, the concentration of the dye is calculated using a modified form
of the Beer-Lambert equation. For these calculations, the instrument considers the absorption
maximum of the dye, the dye-specific extinction coefficient (see Table 2). The dye concentration
is calculated with or without background correction as follows:
(Amax,dye − A320 ) * Ð
C=
εdye * 106
Amax,dye * Đ
C=
εdye * 106
εdye Extinction coefficient of dye in M-1*cm-1
 Frequency of Incorporation (FOI)

FOI is the degree of labeling based on dye incorporation in a labeled nucleic acid sample. It is
generally expressed as the number of dye molecules incorporated per 1000 nucleotides. FOI
can be calculated with or without background/dye correction as follows:
35
With background correction with dye correction:
324.5 * (Amax, dye − A320 )

FOI =
εdye * 106 * (A260 − A320 − cfdye * (Amax,dye − A320 ))
With background correction without dye correction:
324.5 * (Amax, dye − A320 )

FOI =
εdye * 106 * (A260 − A320 ) * εnuc
Without background correction and with dye correction:
324.5 * Amax, dye

FOI = 6
εdye * 10 * (A260 − cfdye * Amax,dye ) * εnuc
Without background correction and without dye correction:
324.5 * Amax, dye

FOI =
εdye * 106 * A260 * εnuc
FOI Frequency of Incorporation (dye per 1,000 bases)

Table 2. Dye Types, Absorbance Max, Extinction coefficient, and dye-dependent

correction factors
NanoPhotometer Dye Type Absorbance Dye-dependent Dye-dependent

Model maximum of ext. coeff. correction factor
Dye (nm) εdye in M-1*cm-1 at 260 nm cfdye
NP80/N60/N50/C40 Alexa Fluor 350 345 18,400 0.25
NP80/N60/C40 Alexa Fluor 647 650 239,000 0.00
36
NP80/N60/C40 Alexa Fluor 660 660 107,000 0.00

NP80/N60/C40 Alexa Fluor 680 680 164,000 0.00
NP80/N60/N50/C40 Cy3 550 150,000 0.08
NP80/N60/N50/C40 Cy3.5 581 150,000 0.08
NP80/N60/C40 Cy5 649 250,000 0.05
NP80/N60/C40 Cy5.5 675 250,000 0.05
NP80/N60/N50/C40 Oyster-500 503 78,000 0.29
NP80/N60/N50/C40 Oyster-550 553 150,000 0.05
NP80/N60/N50/C40 Oyster-556 560 155,000 0.03
NP80/N60/C40 Oyster-645 649 220,000 0.05
NP80/N60/C40 Oyster-650 653 200,000 0.04
NP80/N60/C40 Oyster-656 660 200,000 0.04
NP80/N60/N50/C40 Texas Red 593 85,000 0.23
 Ratios
Reactions utilizing nucleic acids often require minimum purity standards. Common contaminants
of nucleic acid samples include: proteins, organic compounds, and other. Based on the common
contaminants of nucleic acid samples, the 260/280 and 260/230 ratios are calculated for nucleic
acids to give an indication of the purity of the samples. Pure DNA and RNA preparations have
expected 260/280 ratios of  1.8 and  2.0 respectively. An elevated absorbance at 230 nm can
indicate the presence of impurities as well; 230 nm is near the absorbance maximum of peptide
bonds and also indicates buffer contamination since TRIS, EDTA and other buffer salts absorb
at 230nm. When measuring RNA samples, the 260/230 ratio should be > 2.0; a ratio lower than
this is generally indicative of contamination with guanidinium thiocyanate, a reagent commonly
used in RNA purification and which absorbs over the 230 - 260 nm range.
The ratios are calculated with or without background correction according to if the background
correction is activated during the measurements or not as follows:

A260
260/280 ratio = A280
A260
260/230 ratio = A230
A260 - A320
260/280 ratio = A280 - A320
A260 - A320
260/230 ratio = A230 - A320
37
PROTEIN UV
M ETHOD OVERVIEW
The Protein UV method exploits the inherent absorbance of proteins at 280 nm in combination
with the Beer-Lambert Law, where each protein is characterized by a protein specific extinction
coefficient (ε) which can be used to determine total protein concentration of a solution. The
intrinsic absorbance of proteins is due to the presence of aromatic amino acids in their structure,
primarily tryptophan and tyrosine, as well as cysteine (oxidized cysteine residues in a disulphide
bond). The aromatic amino acid residues in a protein containing tryptophan and tyrosine exhibit
strong intrinsic absorbance at 280 nm, with a lesser contribution by phenylalanine. Therefore, it
is the aromatic amino acid residues which dictate the extinction coefficient at 280 nm for a
protein.
The most straightforward method to determine concentration of a purified, homogenous protein

with a known extinction coefficient (ε) is by direct measurement of UV280 provided as long as
the protein contains no prosthetic groups with strong absorption in the same region. However,
for unknown proteins including homogenous protein mixtures, it is possible to make direct A280
measurements using a composite ε value derived from comparison of many proteins, although
this will only provide an approximate but close estimate of the true protein concentration.
The NanoPhotometer determines protein concentration by performing calculations based on

specific ε values, either pre-programmed in the instrument or entered manually by the user.
Extinction coefficient (ε) values at 280 nm vary greatly for different proteins due to their
particular aromatic amino acid content. Fixed ε values are pre-programmed in the software for
certain proteins (see
38
Table 3). However, if the protein of interest is not included in the pre-programed methods it is
also possible to manually enter the specific ε for the protein of interest using the Mol. Ext.
Coefficient or Ext. Coefficient protein option. For correct calculation, it is necessary to supply
either: the mass extinction coefficient (ε in l/g*cm); or b) or the molar extinction coefficient (εM in
M-1*cm-1), and the molecular weight of the protein expressed in molar mass units (g/mol).
To determine the degree of dye labelling of a protein, the absorbance measured at the
wavelength corresponding to the absorbance maximum of the fluorescence dye is used (see
39
Table 3). The corresponding extinction coefficient of the dye is used along with the in the Beer-
Lambert Law to determine the dye concentration.
Note: It is important to ensure the extinction coefficient and units entered are correct in order to
ensure that calculations are performed properly for accurate concentration values.
40
1. Select the Protein UV icon on the home screen.
To change between NanoVolume and cuvette application (NP80/C40 only)
use the Change to Cuvette/NanoVolume button below the parameter area.
2. Select the protein type in the drop-down of the parameter area:

Options are: BSA, SA Mouse, SA Human, IgG Mouse, IgG Human, IgE
Human, Lysozyme, OD1, Mol. Ext. Coefficient, Ext. Coefficient.
 For Mol. Ext. Coefficient enter Molecular Weight (default 66,400 g/mol)
and Mol. Ext. Coefficient (default 44,289 M-1*cm-1)
 For Ext. Coefficient enter Ext. Coefficient (default 0.667 l/g*cm)

Select the volume of sample to be applied.
Note: 1 - 2 µl (default): automatic path length change; 0.3 µl measures only
the 0.07 mm path length (possible for samples with concentrations e.g. BSA
> 12.6 mg/ml)
4. The background correction is enabled as the default. It is possible to disable

the background correction with the toggle switch.
green.
6. If a dye labeled sample is used please add a dye by tapping on the Add Dye
Label option and select a dye from the drop-down list. There is also an
option for dye correction which can be en-/disabled with a toggle switch.
Added Dyes can be deleted by tapping on the delete icon ( ).
Note: If the used dye is not available in the drop-down list, please go to
preferences and add a custom dye to the dye list.
41
preferences.
the measurement.
C ALCULATIONS
 Protein UV280 Concentration
The protein concentration in the Protein UV method is calculated with the absorbance value of
the sample at 280 nm along with the extinction coefficient defined by the user. The protein
concentration is calculated with or without background correction as follows:
C = (A280 − A320 ) * εprot * Ð
C = A280 * εprot * Ð
C Concentration (ng/µl)
εprot Extinction coefficient/protein factor in g*cm/l
Ð Dilution factor
42
Table 3. Protein extinction coefficients (εprot )

-1 -1
Type εprot [ g* cm/l] Ext. Coeff. [l/g*cm] Mol. Ext. Coeff. [M *cm ] MW [g/mol]
BSA 1.50 0.667 44,289 66,400
SA Mouse 1.49 0.670 44,220 66,000
SA Human 1.72 0.582 40,370 69,365
IgG Mouse 0.71 1.400 224,000 160,000
IgG Human 0.74 1.360 204,000 150,000
IgE Human 0.65 1.530 290,700 190,000
Lysozyme 0.38 2.640 37,984 37,984
OD1 1.00 N/A N/A N/A
 Dye-labeled Protein UV280 Concentration

For dye-labeled proteins, the concentration of the protein is calculated using a modified form of
the Beer-Lambert equation. For these calculations, the instrument considers the absorption
maximum of the dye, and a certain dye-specific correction factor at 280 nm (see Table 4). The
dye concentration is calculated with or without background/dye correction for are as follows:
C = [A280 − A320 − cfdye * (Amax,dye − A320 )] * εprot * Ð
With background and without dye correction:
C = (A280 − A320 ) * εprot * Ð
Without background and with dye correction:
C = (𝐴280 − 𝑐𝑓𝑑𝑦𝑒 ∗ 𝐴𝑚𝑎𝑥,𝑑𝑦𝑒 ) * εprot * Ð
Without background and without dye correction:
C = A280 * εprot * Ð
C Concentration in mg/ml
Ð Dilution factor
43
 Dye Concentration
For dye-labeled proteins, the concentration of the dye is calculated using a modified form of the
Beer-Lambert equation. For these calculations, the instrument considers the absorption
maximum of the dye, and a dye-specific extinction coefficient (see Table 4). The dye
concentration is calculated with or without background correction for are as follows:
((Amax,dye − A320 ) * Ð)
C=
εdye * 106
(Amax,dye * Ð)
C=
εdye * 106
C Concentration
Amax, dye Absorbance at the max dye absorbance value (10 mm path)
Ð Dilution factor
 Degree of Labeling (DOL)

DOL is the degree of labeling based on the average number of dye molecules coupled to a
protein molecule. The degree of labeling can be determined from the absorption spectrum of the
labeled antibody with or without background/dye correction as follows:
(Amax, dye − A320) * εprot

DOL =
(A280 − A320 − cfdye * (Amax, dye − A320)) ∗ εdye
With background and w/o dye correction:
(Amax, dye − A320) * εprot

DOL =
(A280 − A320) * εdye
W/o background and with dye correction:
Amax, dye * εprot

DOL =
(A280 − cfdye * Amax, dye ) * εdye
44
W/o background and w/o dye correction:
Amax, dye * εprot

DOL =
A280 * εdye
DOL Degree of labeling/dye per protein ratio

Table 4. Dye Types, Absorbance Max, Extinction coefficients, and dye-dependent

correction factors
NanoPhotometer Dye Type Absorbance Dye-dependent Dye-dependent

Models maximum ext. coeff. correction
of Dye (nm) εdye in M-1*cm-1 factor at 280 nm
cfdye
NP80/N60/C40 Alexa Fluor 647 650 239,000 0.03
NP80/N60/C40 Alexa Fluor 680 679 184,000 0.05
NP80/N60/C40 Alexa Fluor 790 785 260,000 0.08
NP80/N60/N50/C40 Cy3 550 150,000 0.05
NP80/N60/C40 Cy5 649 250,000 0.05
NP80/N60/C40 DyLight 649 654 250,000 0.04
NP80/N60/N50/C40 DyLight 488 493 70,000 0.15
NP80/N60/N50/C40 FITC 495 68,000 0.30
NP80/N60/N50/C40 Pacific Blue 409 30,000 0.20
NP80/N60/N50/C40 Pacific Orange 397 24,500 0.60
NP80/N60/N50/C40 pHrodo Green 505 75,000 0.20
NP80/N60/N50/C40 pHrodo Red 560 65,000 0.12
NP80/N60/N50/C40 r-PE 566 200,000 0.18
NP80/N60/N50/C40 Texas Red 595 80,000 0.18
45
PROTEIN ASSAYS
M ETHOD OVERVIEW
Protein concentration may be measured using colorimetric assays, in which certain reagents are
added to the protein solution to generate a colored product; either a protein-cupric ion chelate
as in the Biuret, Lowry, BCA assays or a protein-dye complex as in the Bradford assay. In these
colorimetric assays, the absorbance is measured in the visible range at the appropriate
wavelength for each assay and compared against a standard curve prepared by serial dilution
of a protein standard of known concentration. A linear regression analysis of the calibration
standard data points is calculated by the NanoPhotometer. A correlation coefficient (R2) in the
range of 0.95 to 1.00 indicates a good fit to a straight line.
 Bradford Assay
Method depends on quantifying the binding of a dye, Coomassie Brilliant Blue, to an unknown
protein and comparing this binding to that of a standard curve prepared from a set of known
protein of known concentrations at 595 nm. This standard is usually BSA (bovine serum
albumin).
 Biuret Assay
Method depends on a reaction between cupric ions and peptide bonds in an alkali solution,
resulting in the formation of a complex absorbing at 546 nm.
 BCA Assay
Method depends on a reaction between cupric ions and peptide bonds coupled with the
detection of cuprous ions using bicinchoninic acid (BCA), giving an absorbance maximum at
562 nm. The BCA process is less sensitive to the presence of detergents used to solubilize
membranes.
 Lowry Assay
Method is based on the Biuret reaction. Under alkaline conditions the divalent copper ion forms
a complex with peptide bonds in which it is reduced to a monovalent ion. Monovalent copper ion
and the radical groups of tyrosine, tryptophan, and cysteine react with Folin reagent to produce
an unstable product that becomes reduced to molybdenum/tungsten blue. The bound reagent
changes color from yellow to blue. This binding is compared with that obtained with a standard
protein at 750 nm; this is usually BSA (bovine serum albumin).
Note: Detailed protocols are customarily supplied with these assay kits, and must be closely
followed to ensure that accurate results are obtained.
46
Note: It is not recommended to use the NanoVolume application for Protein Assays. For best
results use the cuvette mode (NP80 and C40 models only) for the Protein Assays.
1. Select protein assays icon from home screen.

To change between NanoVolume and cuvette application, use the Change
to Cuvette/NanoVolume button below the parameter area (NP80/C40 only).
2. Select protein assay type from drop-down of the parameter area.

Options are: BCA Assay, Bradford Assay, Lowry Assay, Biuret Assay
3. For Cuvette Application:

For NanoVolume Application:
Select the dilution depending on the sample concentration
Note: There is no automatic path length setting available in this method.
Select either a virtual dilution of 15 (path length 0.67 mm) or of 140 (path
length 0.07 mm).
green.
5. The baseline correction is disabled as the default. It is possible to choose

between different wavelengths for the baseline correction.
Options are: 377 nm, 604 nm, 770 nm (not N50) and 823 nm (not N50)
6. Select the curve fit type: Options are linear regression and zero regression
(forces the straight line through the origin)
7. Standard new (no selection possible)
47
New:
Add up to 20 Concentrations and choose Replicates none, 2 or 3.
Measure a blank and depending on the replicate setting all concentrations.

Results will be shown in the results area and if replicates are selected a
mean value is shown. It is possible to exclude single measurements from
the curve calculation by switching the toggle switch off.
Note: The standard curve cannot be altered any longer once the first
sample is measured.
8. Once Standard curve is created or loaded it will be used for concentration

calculations in the method. It might be necessary to do a blank
measurement
Note: Use for NanoVolume measurements always a minimum of 1 µl for
any blank measurement.
9. Apply sample and press the sample button to initiate the measurement.
Note: Once the sample measurement is initiated it is not possible to do
changes to the standard curve.
C ALCULATIONS
Protein concentration is determined using the standard curve by correlating absorbance values
of samples with known concentration to calculate the concentration of the unknown sample. In
order to maintain accuracy and precision please ensure that the R2 value of the standard curve
is 0.95 or greater.
KINETICS
Please contact the Implen support for further details.
48
OD600
M ETHOD OVERVIEW
The growth of bacteria in liquid culture media is commonly monitored by measuring the optical
density at 600 nm (OD600) in small samples taken from the cultures. OD600 measurements are
typically used to determine the stage of growth of the bacterial culture, thereby ensuring that
cells are harvested at an optimum point that corresponds to an appropriate density of live cells.
Growth of bacterial cells typically progresses through a series of consecutive phases including:
lag, log, stationary and decline (see Figure 1). In general, cells should be harvested towards the
end of the log phase using the optical density of the samples to determine when this point has
been reached. Since optical density in the case of OD600 measurements results from light
scattering rather than light absorption, this value varies depending on the type of bacterial cells
in the culture in terms of size and shape. Cells are routinely grown until the absorbance at 600
nm (known as OD 600) reaches approximately 0.4 prior to induction or harvesting. A linear
relationship exists between cell number (density) and OD 600 up to an absorbance value of 0.6,
approximately.
As mentioned above, for turbid samples such as cell cultures, the absorbance measured is due
to light scattering, and not the result of molecular absorption. Since the extent of scattering is
affected by the optics of the system (distance between the cell holder and instrument exit slit,
monochromator optics, slit geometry, etc.), different spectrophotometer types will tend to give
different OD 600 readings for the same turbid sample. Therefore, if results from different
spectrophotometers are to be compared, they must be normalized first using appropriate
calibration curves.
A calibration curve can be constructed by comparing measured OD 600 to expected OD 600.

Expected OD 600 is determined by counting cell number using an alternative technique (for
example microscope slide method) and converting to OD 600 using the rule of thumb that 1 OD
600 = 5 x 108 cells/ml for E. coli.
The NanoPhotometer comes with a correction factor of 1 as default. To compare OD 600 values
between different spectrophotometers, it is necessary to determine the constant deviation or
ratio between the absorbance values for the same sample from each instrument and use this
factor within the setting “correction factor” of your NanoPhotometer Software.
Note: The use of 10 mm path length disposable cells is recommended for optical density
measurements of cell culture solutions. Also, to prevent the suspension settling too quickly and
giving an OD reading that changes with time, glycerol should be added to the sample.
49
Figure 1 Bacterial growth curve
Note: It is not recommended to use the NanoVolume application for the OD600 application. For
best results use the cuvette mode (NP80 and C40 models only) for OD600 measurements.
1. Select the OD600 icon on the home screen
2. For Cuvette Application:

For NanoVolume Application:
Note: There is no automatic path length setting in this method. Select either
a virtual dilution of 15 (path length 0.67 mm) or of 140 (path length 0.07 mm)
3. If it is desired to heat the cuvette compartment to 37°C turn the toggle switch
on for heated cuvette. Once the cuvette reaches the desired temperature the
switch will turn from orange to green.
4. Default wavelength is 600 nm but can be changed, depending on the

application.
5. Toggle switch cells/ml is default disabled. Enable cells/ml to get the cells/ml
calculated. Enter the cell specific factor and multiplier (e.g. 1 OD600 = 5 x
108 cells/ml)
6. Enter the correction factor to compensate for different optical configurations

between this and other instruments
7. Option to smooth the graph with different boxcars. off, 1 = boxcar 11

(default), 2 = boxcar 21 and 3 = boxcar 61
50
9. Insert cuvette with the reference sample and select blank button to initiate
the measurement
Note: Use for NanoVolume measurements always a minimum of 1 µl for any
blank measurement.
10. Insert cuvette with the sample and select the sample button to initiate
the measurement
C ALCULATIONS
OD600 = A600 * Ð * cf
OD600 Optical density at 600 nm

Ð Dilution factor
cf Correction factor for spectrophotometer
Cells⁄ml = A600 * Ð * cf * multiplier

Ð Dilution factor
cf Correction factor for spectrophotometer
multiplier Multiplier of sample
MORE APPS
The More Apps icon located on the home screen opens another menu screen with access to
icons for additional applications available on the NanoPhotometer. The applications featured in
this menu include: wavelength, concentration, wavescan, absorbance/ratio, standard curve and
custom applications.
MORE APPS: WAVELENGTH

M ETHOD OVERVIEW
In the wavelength application it is possible to measure simple absorbance (A) and %
transmittance (%Trans. / only in cuvette mode) of a sample at specific wavelengths. It is
possible to add up to 20 different wavelengths
51
M EASUREMENT PROTOCOL
1. Select the More Apps icon from the Home screen and then the
Wavelength icon from the More Apps screen

3. If it is desired to heat the sample to 37°C use the toggle switch to turn on cell
holder heater. When the cuvette holder has 37°C the color changes to
green.
4. Enter desired wavelength () to be measured. It is possible to measure up to

20 wavelengths simultaneously. More wavelength () options are added by
selecting the wavelength button. The added wavelength can be deleted with
5. Baseline correction is default off and can be enabled by selecting the

different values for the correction in the drop-down menu: 377 nm, 604 nm,
770 nm (N/A N50) and 823 nm (N/A N50)

preferences.
52
10.Apply sample to the sample window and press the sample button to initiate
the measurement.
C ALCULATIONS
 Absorbance Calculation:
Absorbance is formally defined as the decimal logarithm (base 10) of the reciprocal of
transmittance:
1
A = log ( ) = - log T
T
T = 10(-A)
Note: Corresponding absorbance value e.g. Absorbance value ( = 230) etc. normalized to 10
mm path length
 %Transmittance Calculations (cuvette mode only)

In the wavelength application it is possible to measure the absorbance (A) and % transmittance
(%T) on a sample with respect to a reference at a specific wavelength. Transmittance is the
ratio of light intensity remaining after it has passed through the sample (I) to the initial incident
light intensity (I0):
𝐼
𝑇=
𝐼0
𝐼
%𝑇 = × 100
𝐼0
MORE APPS: WAVESCAN

M ETHOD OVERVIEW
Using the wavescan application it is possible to obtain the complete spectral scan for a defined
wavelength range between 200 - 900 nm (NP80/N60/C40) or from 200 - 650 nm (N50).
53
Wavescan icon from the More Apps screen

Note: There is no automatic path length setting in this method. Select
either a virtual dilution of 15 (path length 0.67 mm) or of 140 (path length
0.07 mm)
green.
4. Set desired wavelength range (Start and End Wavelength) to be scanned

for the samples.
Note: If samples with a different wavelength range are selected, the graphs
are shown on the full scan range of 200 – 900 nm (N50: 200-650 nm)
5. Baseline correction is off as the default and can be enabled by selecting

the different values for the correction in the drop-down menu: 377 nm, 604
nm, 770 nm (N/A N50) and 823 nm (N/A N50)

preferences.
54
the measurement.
C ALCULATIONS
No calculations necessary, values are reported based on 10 mm path length.
In the results are the five prominent peaks shown with wavelength and absorbance value. For
cuvette measurements it is possible to change to the %Transmittance mode. If a peak of
interest is not shown in the results the peak can be added by clicking on the graph and added to
the results by tapping on the Add Peak button in the pop-up window:
MORE APPS: ABSORBANCE RATIO

M ETHOD OVERVIEW
In this mode, it is possible to determine simple absorbance ratios for a given sample by
measuring the absorbance at two wavelengths specified in the parameters of the method
relative to a blank.
Absorbance/Ratio icon from the More Apps screen

0.07 mm)
55
green.
4. Enter desired wavelengths ( 1-1 and  1-2) for ratio calculation. It is

possible to measure up to 20 absorbance/ratios simultaneously. More
wavelength for ratio calculation can be added by selecting the Add Ratio
button. The added ratios can be deleted with


preferences.
the measurement.
56
C ALCULATIONS
The absorbance ratio is calculated from the two path lengths specified by the user in the
parameters.
λ1
λ1 : λ2 =
λ2
λ1 : λ2 = Absorbance Ratio
λ1 = Absorbance 1 corresponding absorbance value 1 selected normalized to 10 mm path
λ2 = Absorbance 2 corresponding absorbance value 2 selected normalized to 10 mm path
MORE APPS: CONCENTRATION

M ETHOD OVERVIEW
In this mode, concentration can be calculated for a sample by determining the absorbance at a
specific wavelength relative to a reference. The concentration is then obtained by multiplying the
measured absorbance by a specific factor. This factor may be known in advance and entered by
the user, or it may be calculated by the instrument by measuring a set of standard (standard
curve method) with known concentrations to create a standard curve.
Concentration icon from the More Apps screen.

0.07 mm)
green.
4. Default wavelength is 260 nm but can be changed, depending on the

application.
5. Enter a factor for concentration calculation
57


preferences.
11. Apply sample to the sample window and press the sample button to
initiate the measurement.
C ALCULATIONS
In this method, the concentration of the sample is calculated based on the Beer-Lambert law
given the user specified wavelength of interest and user defined extinction coefficient. The
equations for calculating concentration with and without background correction are as follows:
𝐶 = 𝐴𝑛 ∗ ε ∗ Ð
C Concentration (ng/µl)
𝐴𝑛 Absorbance at user specified path length n (10 mm path)
Ð Dilution factor
ε extinction coefficient/factor
58
MORE APPS: STANDARD CURVE

M ETHOD OVERVIEW
The construction of a calibration curve from multiple standards of known concentrations can be
created and stored on the NanoPhotometer. The standard curve can be used to quantify
samples of the same type with unknown concentrations. This application provides an extremely
useful tool with which to integrate, expedite and simplify the measurement and calculations
involved in determining the concentration of analytes in unknown samples. If a zero
concentration standard is required, include it in the number of standards to be entered using a
reagent blank and entering 0.00 for concentration.
1. Select the More Apps icon from the Home screen and then the Standard
Curve icon from the More Apps screen.

green.
4. The baseline correction is disabled as the default. It is possible to choose

between different wavelengths for the baseline correction.
Options are: 377 nm, 604 nm, 770 nm (N/A N50) and 823 nm (N/A N50)
5. Select the curve fit type: Options are linear regression and zero regression
(forces the straight line through the origin)
59
6. Standard new no selection possible
New:
Add up to 20 Concentrations and choose Replicates none, 2 or 3.
Measure a blank and depending on the replicate setting all concentrations.

Absorbances will be shown in the results area and if replicates are selected
a mean value is shown. It is possible to exclude single measurements from
the curve calculation by switching the toggle switch off.
Note: The standard curve cannot be altered any longer once the first
sample is measured.
7. Once Standard curve is created or loaded it will be used for concentration

calculations in the method. It might be necessary to do a blank
measurement.
Note: Use for NanoVolume measurements always a minimum of 1 µl for
any blank measurement.
8. Apply sample and press the sample button to initiate the measurement.
Note: Once the sample measurement is initiated it is not possible to do
changes to the standard curve.
C ALCULATIONS
Concentration is determined via the absorbance values provided by the standard curve based
on the curve fit selection including the following options: linear regression or zero
regression.
CUSTOM APPS
There is an option for designing customer specific Custom Apps which can be loaded to the
NanoPhotometer. For more information about designing custom applications to suit individual
research needs please contact Implen directly for assistance.
60
STORED RESULTS
The Stored Results icon opens the directories of folders containing files of results that have
been previously saved.
On the left side of the screen all available directories/folders are shown: NanoPhotometer,
Control Device and/or USB flash drive. To open a folder click on the  icon, for selecting the
folder click on the folder name.
Folder can be created by tapping on . Folders can be deleted, renamed, moved or copied to
by clicking on the icon.
On the right side of the screen all saved result files of the selected folder are shown and can be
opened by a long or double click.
It is also possible to delete, rename, move or copy files by clicking on the icon.
Note: Control device is only available on tablets and smartphones not on the NanoPhotometer
and computer versions of the software.
61
STORED METHODS
The stored methods icon opens the directories of folders containing methods stored by the user.
On the left side of the screen all available directories are shown: NanoPhotometer and/or USB
flash drive. To open a folder click on the  icon, for selecting the folder click on the folder name.
New folders can be created by clicking on . Folders can be deleted, renamed, moved or
copied to by clicking on the icon.
On the right side of the screen all saved methods of the selected folder are shown and can be
opened by a long or double click.
It is also possible to delete, rename, move or copy methods by clicking on the icon.
62
5. PREFERENCES
System preferences can be set by selecting preferences ( ) on the home screen. The
preferences menu includes: general, dyes and network. The menu item which is selected will
have its preference options listed in the window to the right.
Note: Preferences are not available for smart phone < 7” screen versions.
GENERAL
Selecting General in the Preferences menu opens a window to the right of the preferences
menu with the following options: Date & Time, Region, Display (built-in display only), Statistics,
About and Illumination Sample Window.
DISPLAY
The brightness of the built-in screen can be adjusted under display.
Note: Display preferences are only available for instruments with integrated touchscreen.
ABOUT
In about the following information about the NanoPhotometer are shown: NanoPhotometer
model, serial number, IP address, hardware version, firmware version and software.
WIFI ACCESS POINT

Toggle Switch to en-/disable the WiFi access point.
ILLUMINATION S AMPLE WINDOW

Toggle switch to switch on/off the illumination of the sample window.
Note: Only available for NP80/N60/N50 models.
DYES
There is a list of available dye-labels for both nucleic acid dye and protein dye methods. Each
dye has either an ( ) icon in front of the dye name indicating that the dye is locked and cannot
be changed or deleted. If the dye has a delete symbol ( ), there is an option to delete the dye
which is not locked or pre-programmed into the NanoPhotometer.
Selecting a dye name opens a new screen with the dye information: dye name, absorbance
maximum dye (nm), dye-dependent extinction coefficient εdye (M-1 * cm-1), and dye-dependent
correction factor as well as the option to show the dye in the drop-down of the application
(Nucleic Acid or Protein UV).
63
Note: It is not possible to delete a dye of the factory list; custom dyes can be deleted if they are
not locked.
It is possible to add a new dye to the list by selecting the button to add a new dye. A window
will open where it is possible to enter the: dye name, dye absorbance maximum (nm), dye-
dependent extinction coefficient εdye (M-1 * cm-1), and dye-dependent correction factor. There is a
toggle switch available to lock the dye to prevent deleting a dye from the dye list accidentally.
6. TROUBLESHOOTING
SELF-CALIBRATION TEST
The NanoPhotometer self-calibration test is performed automatically every time the instrument
is powered on. If the instrument passes the self-calibration test the home screen is shown. If the
instrument does not pass the test, a window with a message will appear along with the message
explaining the reason for the failed test along with the recommended solution. If the ok button is
selected, the window is closed and the home screen will be shown with an error message at the
top. The error message is also shown on top of all other screen and all performed
measurements including the saved files of those measurements. If the self-calibration test fails
please contact the Implen Support Team.
7. ASSISTANCE
The Assistance menu includes: support, report a problem (only available for tablet and
computer versions), software maintenance and legal as functions to help with any technical
issues or questions that may arise with the NanoPhotometer. The menu list item selected on the
left side assistance menu will appear in the window to the right.
Note: Assistance function is not available for smart phone < 7” screen versions.
64
SUPPORT
Selecting support on the left side assistance menu will show the available options for contacting
Implen.
REPORT PROBLEM
The function to report a problem is available on computer and tablet versions only. When report
a problem is highlighted in the left side assistance menu, the right side will have a form to fill out
with information including: first name, last name, phone number, email, and country. A drop-
down menu provides the option to select the problem type and includes the following selections:
error message, software, firmware, measurements, and other. It is also possible to enter a
question or comment at the end of the form. Once the form is completed and the send button is
selected a message will be sent directly to Implen and the appropriate support person will
contact as soon as possible to provide further support.
Note: The report a problem function is only available for computer and tablet versions.
SOFTWARE MAINTENANCE
RESET
There is an option to reset the instrument to factory settings. By selecting the reset button a
window will open that says “Would you like to reset the NanoPhotometer?” Selecting the cancel
button will close the window without changing the settings and selecting reset will open a
window that will ask again” Would you really like to reset the NanoPhotometer to factory
settings?” If it is confirmed the factory settings will be restored.
Note: All stored methods, settings and data on the NanoPhotometer will be deleted if the reset
option is executed.
65
SOFTWARE UPDATE
There is a button for software update. It is needed to plug in a USB flash drive with the software
installation file to the USB port. The software update files are available on the Implen
homepage: www.implen.de.
Update procedure:
1. Copy the NPOS.bin file to a USB flash drive
2. Plug in the USB flash drive to the USB port of the NanoPhotometer
3. Go to Assistance/Software Maintenance
4. Press the Update button. The update will start and once finished automatically reboot the
NanoPhotometer.
Note: Make sure that the NanoPhotometer is connected to power and that the power
connection is not interrupted during the update.
CONTACT IMPLEN
There is an option to contact Implen for instruments connected to the internet. For any support
issues and questions please contact the Implen team directly:
Europe, Asia, South Pacific, Middle East and Africa

Implen GmbH
Schatzbogen 52
81829 München
Germany
Phone: +49 89 72637180

Fax +49 89 726371854
Email: [email protected]
www.implen.de
North and South America

Implen, Inc.
Unit 104
31194 La Baya Drive
Westlake Village, CA 91362
USA
Phone +1 818 748-6400

Telefax +1 818 449-0416
Email: [email protected]
Website www.implen.com
66
8. MAINTENANCE
MAINTENANCE FREE TECHNOLOGY
The NanoPhotometer technology is maintenance-free. Regular maintenance and calibration is
not necessary.
For facilities that are working according to national as well as international guidelines and
standards including: Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), or
ISO9000-9004; the proper performance of the spectrophotometer has to be tested and proven
on a regular basis with individually set intervals. Implen provides certified NanoPhotometer
secondary standards as an optional accessory. These NanoPhotometer Didymium glass filters
and standard solution sets are suitable for the control and documentation of the wavelength
accuracy and the photometric accuracy of your system. IQ/OQ documentation is also available.
Please contact your local Implen office or an authorized Implen partner for further information.
Support agreements that help to fulfill the demands of regulatory guidelines concerning
GLP/GMP include: calibration certification using filters traceable to international standards
(during production and quality control), certified engineers and calibrated test equipment,
approved to ISO 9001 standard, automatic self-diagnostic calibration test during start of the
NanoPhotometer, result is documented in each data output file, and possibility to save a Implen
Document Source (IDS) file (no data manipulation possible).
REPLACEMENT PARTS
 Lamp Replacement
The NanoPhotometer is equipped with a xenon flash lamp and should not need replacement
until several years of use. In the unlikely event the lamp does need to be replaced, this should
be done by the manufacturer or a certified service engineer from your supplier.
 Battery Replacement
The optional battery pack can only be assembled or replaced by the manufacturer or a certified
service engineer from your supplier.
Note: Danger of explosion if battery is incorrectly replaced. Replacement only with the same or
equivalent type recommended by the manufacturer: Replacement needs to be done by a
certified service engineer
 Touchscreen Replacement
The optional touchscreen can only be assembled or replaced by the manufacturer or a certified
service engineer from your supplier.
67
CLEANING AND GENERAL CARE

Switch off the NanoPhotometer and disconnect the power cord prior to external cleaning. Use a
soft wet cloth or dry microfiber cloth to clean all external surfaces. A mild liquid detergent may
be used to remove stubborn marks.
Approved disinfectant solutions include: Apesin disinfection spray (Tana Chemi GmbH), Incidin
Liquid & Inciddin Foam (Ecolab), and Lysoformin Spezial (Lysoform Dr. Hans Roseman GmbH).
Note: Observe all necessary precautions if dealing with hazardous samples or solvents.
9. WARRANTY
Implen guarantees that the product supplied has been thoroughly tested to ensure that it meets
its published specification. The warranty included in the conditions of supply is valid for 12
months and is valid only if the product has been used according to the instructions supplied.
Implen or your supplier can accept no liability of loss or damage arising from the faulty or
incorrect use of this product
68
10. ALPHABETICAL APPENDIX

A
H
Absorbance Ratio..................................................... 53
Calculations ......................................................... 55 HDMI ........................................................................ 14
Measurement Protocol ......................................... 53
Accessories ........................................................ 11–13 I
Assistance ................................................................ 62
Maintenance ........................................................ 63 Icons ........................................................................ 22
Report Problem.................................................... 63 IDS files .................................................................... 26
Support ................................................................ 63 Installation
Software .............................................................. 18
Spectrophotometer .............................................. 16
B
Battery................................................................ 17, 65 L
BCA Assay ............................................................... 44
Biuret Assay ............................................................. 44 Lamp ........................................................................ 65
Bradford Assay......................................................... 44 LAN .......................................................................... 14
Buttons ..................................................................... 22 Lowry Assay ............................................................. 44
C M
Cleaning ................................................................... 66 Maintenance............................................................. 65
Compatibility............................................................. 18 Measurement
Solvent ................................................................. 30 Cuvette .......................................................... 28, 30
Concentration ........................................................... 55 NanoVolume .................................................. 27, 29
Calculations ......................................................... 56 More Apps ................................................................ 49
Measurements Protocol ....................................... 55 Absorbance Ratio ................................................ 53
Connecting Cable..................................................... 12 Concentration ...................................................... 55
Connectivity ............................................................. 14 Standard Curve.................................................... 57
Contact ..................................................................... 64 Wavelength .......................................................... 49
Custom Apps............................................................ 58 Wavescan ............................................................ 51
Cuvette ............................................................... 28, 30
N
D NanoPhotometer C40 ............................................. 10
Delete Data .............................................................. 26 NanoPhotometer N50 ............................................... 9
Didymium Glass Filter .............................................. 12 NanoPhotometer N60 ............................................... 8
DiluCell ..................................................................... 13 NanoPhotometer NP80 ............................................ 7
NanoVolume ...................................................... 27, 29
NPOS ....................................................................... 18
E Nucleic Acids............................................................ 32
Excel ........................................................................ 26 Calculations ......................................................... 33
Measurements Protocol ....................................... 32
F
O
Field Kit .................................................................... 13
OD600 ...................................................................... 47
Calculations ......................................................... 49
G Measurements Protocol ....................................... 48
Graph area ............................................................... 24
Graph Overlay .......................................................... 24
69
P Update ................................................................. 64
Solvent Compatibility................................................ 30
Parameter area ........................................................ 24 Standard Curve ........................................................ 57
Positioning ............................................................... 17 Calculations ......................................................... 58
Power Adapter ......................................................... 12 Measurements Protocol ....................................... 57
Preferences .............................................................. 61 Stored Methods ........................................................ 60
Dyes .................................................................... 61 Stored Results.......................................................... 59
General ................................................................ 61 Submicroliter Cell ............................................... 13, 23
Protein Assay
Calculations ......................................................... 46 T
Measurements Protocol ....................................... 45
Protein Assays ......................................................... 44 Table area ................................................................ 24
Protein UV ................................................................ 38 Technical Specifications ..................................... 14–16
Calculations ......................................................... 40 Touch Screen ........................................................... 65
Measurements Protocol ....................................... 39 Troubleshooting ....................................................... 62
R U
Rear Panel ............................................................... 11 Unpacking ................................................................ 17
Replacement Parts................................................... 65 Update ..................................................................... 64
Battery ................................................................. 65 USB.......................................................................... 14
Lamp.................................................................... 65
Touch Screen ...................................................... 65 W
Reset........................................................................ 63
Results area ............................................................. 24 Warranty .................................................................. 66
Wavelength .............................................................. 49
S Calculations ......................................................... 51
Measurement Protocol ......................................... 50
Safety Information .................................................... 16 Wavescan ................................................................ 51
Save Data ................................................................ 25 Calculations ......................................................... 53
Software Measurement Protocol ......................................... 52
Reset ................................................................... 63 WiFi .......................................................................... 14
70

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NanoPhotometer NP80/N60/N50/C40

Declaration of conformity for the NanoPhotometer (C40/N50/N60/NP80)

2014/35/EU Low Voltage Equipment Safety Directive

2004/108/EC EMC Directive

IEC 60529 Protection class IP20

2002/95/EC Restrictions on the use of certain Hazardous Substances

2012/19/EU EC Directive on Waste Electrical and Electronic Equipment (WEEE)

FCC 47 CFR Part15 §15.107 and §15.109

IEC 62133 and UN38.3 Battery certification and transport test

Standards to which conformity is declared, where relent, are as follows:

EN61326-1:2013 Electromagnetic compatibility- generic emission standard electrical

Dr. Thomas Sahiri

3. NANOPHOTOMETER BASICS ................................................................................ 20

4. NANOPHOTOMETER APPLICATIONS ..................................................................... 32

MEASUREMENTS PROTOCOL ............................................................................................................. 32

10. ALPHABETICAL APPENDIX ................................................................................... 69

Item Number Touchscreen Battery Pack

Item Number Touchscreen Battery Pack

Item Number Touchscreen Battery Pack

Item Number Touchscreen Battery Pack

INSTRUMENT REAR PANEL (NP80/N60/N50/C40)

INSTRUMENT BOTTOM VIEW (NP80/N60/N50/C40)

 NanoPhotometer Power Adapter

The certified didymium glass filter is used as a control of

 Submicroliter Cell (C40 only)

 DiluCell (C40/NP80 only)

Note: Delivered w/o NanoPhotometer and accessories

Processing Power and Compatibility

Do not expose the NanoPhotometer to strong magnetic or electrical fields.

Do not place objects on top of your NanoPhotometer.

 Unpacking and Positioning

REQUIREMENTS AND COMPATIBILITY

Compatible Control Devices

INSTALLING SOFTWARE ON COMPUTER

INSTALLING NANOPHOTOMETER APP ON TABLET OR SMART PHONE

FIRST STEPS AND CONFIGURATION WIZARD

Method Icons Description

Protein UV Protein UV determination at 280 nm (or in a range of 200 -

Kinetics Time vs. Absorbance readings

OD600* Measures cell density at 600 nm (or in a range of 200 – 900

Stored Methods Collection of stored custom methods

Stored Results Archive of stored results

More Apps Additional applications found on a secondary method screen

Define one or multiple wavelength between

Define desired full scan range anywhere between

Define extinction coefficient for automatic

Absorbance/ Define two wavelengths for a calculated absorbance/

Standard Curve Create a standard curve at a defined wavelength

Optional custom applications for personalized

Assistance Opens the assistance page

Preferences Opens the preferences page

Returns to the home screen with application icons for method

Leave Method Returns to the previous application selection

Back Returns to the previous page (smart phone only)

Delete Deletes added functions in parameter; empties input windows

Delete Data Opens a delete dialog pop up

Save Data Opens a save dialog pop up

Add Folder Adds a new folder to the directory

Opens a dialog pop up with several action options including delete,

Full Scale Restores graph to original size without zoom