Chromatograp Hy: Tranninhg Report ON
Chromatograp Hy: Tranninhg Report ON
Chromatograp Hy: Tranninhg Report ON
ON
chromatograp
hy
Under Supervision Submitted by
Dr. Arvind Gupta Jaiprakash Saini
(Senior scientist) B.sc Biotech(Int.)3ed year
Submitted to
Lords International collage Chikani, Alwar
Chromatography is the
separation of a mixture into
individual components using
a stationary and a mobile
phase.
Chromatography Equipment
1. Solvent Tank
2. Pump
3. Feed injection
4. Oven
5. Detector
1. GAS-LIQUID
CHROMATOGRAPHY
2.COLUMN CHROMATOGRAPHY
3.THIN LAYER
CHROMATOGRAPHY
4.HIGH PRESSURE LIQUID
CHROMATOGRAPHY
5.ION EXCHANGE
CHROMATOGRAPHY
Gas- liquid Chromatography Which
the mobile phase is carrier gas
Stationary phase is a microscopic
liquid on an inert solid support, inside
glass or metal tubing called a Colum.
And this instrument used to perform
gas Chromatographic separations is
called a gas Chromatography
(TLC) is a chromatography
technique used to separate
mixtures. Thin layer
chromatography is performed on
a sheet of glass, plastic, or
aluminum foil, which is coated
with a thin layer of adsorbent
material, usually silica gel,
aluminium oxide, or cellulose.
This layer of adsorbent is known
as the stationary phase.
•High performance liquid
chromatography (or high
pressure liquid
chromatography, HPLC) is a
form of column chromatography
used frequently inbiochemistry
and analytical chemistry to
separate, identify, and quantify
compounds based on their
idiosyncratic polarities and
interactions with the column's
stationary phase.
•Ion-exchange chromatography (or ion
chromatography) is a process that allows the
separation of ions and polar molecules
based on their charge. It can be used for
almost any kind of charged molecule
including large proteins, small nucleotides
and amino acids. The solution to be injected
is usually called a sample, and the
individually separated components are
called analytes. It is often used in protein
purification, water analysis, and quality
control.
Affinity chromatography is
a method of
separating biochemical mixtu
res, based on a highly
specific biological interaction
such as that between antigen
and antibody, enzyme
and substrate,
or receptor and ligand