NAME

NAME: SHAHID JAMAL
NEPTUNE CODE: GDWKUX

SDS – PAGE
AIM : To perform SDS -PAGE
INTRODUCTION
Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS – PAGE ) is a technique used
in biochemistry, genetics and molecular biology to separate protein according to their molecular
weight.
The purpose of SDS -PAGE is to separa te protein according to their molecular weight .As
proteins are amphoteric in nature their net charge therefore can be determined by the pH of the
medium in which they are suspended. Therefore at a given pH and under non denaturing
conditions the electroph oretic separations of proteins is determined by both size and charge of
molecules. As proteins are high molecular weight molecules they need a porous gel to get
separated that is why polyacrylamide is used.
MATERIALS REQUIRED:
Acrylamide solution,gel loadi ng buffer,running buffer,staining and destaining
solution,ammonium persulphate,molecular weight marker,protein samples, 10% SDS, 1.5 Tris –
HCL(pH=8.8),0.5m Tris -HCL(pH=6.8),50% glycerol,10%, ?-mercapthanol,0.03% Bromophenol
blue.
Tank with lid, combs, glass plates with spacer, short plates, casting frames, sample loading
guide, casting stands.

METHODS
1.Wash the glass plates with hot water using a detergents
2.Wash off all detergents with ple nty of hot waters and after this stands glass plates in vertical
position to dry(Precaution: always wear gloves to avoid fingerprints on the glass plates)

PREPARATIONS OF SDS -Polyacrylamide gel
we prepare a two types of gel that is stacking gel with large pore on the top and resolving gel
with small por e

Sample and electrophoresis buffe r

STEPS OF ELECTROPHORESIS
1.Making of separating gel
-Hold two glass plates in the casting frame on the casting stands
-Pipette appropriate amount of prepared separating gel solution into the gap between the glass
plates.
-To make the top of the separat ing gel horizontal, fill the water in the gap of the glass till it
overflows.
-Now after this keep the gel for 20 -30 min to be gelate

2.Making of stacking gel
-Before pipeting the stacking gel solution discard the water and we can see the separating gel
clearly
-Now start pipeting the stacking gel solution until it start overflows
-Insert the comb into the gel for making the well withoiut trapping air under the teeth of combs
-Again wait for 20 -30 minutes to become it gelatinised
3.Before taki ng out the comb make sure a complete gelation of the stacking gel.
4.Take out the glass plates from the casting frame and set them in the buffer tank
5.Pour the running buffer into inner and outer chamber.
6.Now prepare your protien sample and mix the samp le with sample buffer.
Heat them at 95?c for 5 minutes
7.Start loading the prepare sample into well and make sure not to overflow.
Don’t forget loading protien marker into the first lane
8.After this now cover the top and connects the anode.Set the appr opriate volt and run the
electrophoresis

The total running time 16h for 120v at 4?c

9.Dye the gel using CBB -R250

RESULTS

Lane 6 is unknown protien by comparing with the lane 10 of the ladder( 10kDa -180kDa).I
concluded that my protien size is 55kDa .

CONCLUSION
Protien staining in the gel creates a documentable banding pattern of the various protiens.
Glycoprotien have differential level of glycosylation and absorb SDS more unevenly at the
glycosylation site resulting in broader and blurred band s.
SDS -PAGE is used in the combination with the western blot for the determination of the
presence of a specific protien in a mixture of protiens or for the analysis of post translational
modification.

55kDa
55kDa
1 2 3 4 5 6 7 8 9 10