TECHNIQUE is to set up gel plates before you mix the gel mixes. Use the THIN spacers and choose a comb--number of wells varies. Make both resolving gel and stack (NO APS or TEMED)--then add APS and TEMED to resolving gel, mix and pour about 3-3.5ml per gel. Before it polymerises, now add APS and TEMED to your stack mix and pour it gently on top of the resolv. gel (using a pasteur pipette works well). Put in the comb and let solidify. Should take 15-20 minutes. You can keep gels overnight at 4℃ if well wrapped to prevent drying out and if you keep the comb in. Note: just before you want to load gels, wash out wells with distilled water to remove unpolymerised acrylamide.

GEL RECEPIES (enough for 2 thin mini-gels)

RESOLVING GEL (NOTE pH 8.8)

Percentage of gel	8%	10%	12.5%
30: 0.8% w/v acrylamide:bisacrylamide	2ml	2.5ml	3.1ml
1.0M Tris-Cl pH 8.8	3ml	3ml	3ml
20% SDS	38ul	38ul	38ul
dH2O	2.43ml	1.9ml	1.3ml
Mix together. Add APS and TEMED just before pouring	.	.	.

10% APS	36ul	36ul	36ul
TEMED	5ul	5ul	5ul
.	7.5ml	7.5ml	7.5ml

STACKING GEL (NOTE pH 6.8)--use 4% stack for <10% res. gel and 6% stack (easier to handle) for >10% resolving gels.

Percentage of stack	4%	6%
30:0.8% w/v acryl:bisacryl	660 ul	1ml
1M Tris-Cl pH6.8	630 ul	630 ul
20% SDS	25 ul	25 ul
dH2O	3.6 ml	3.6 ml
Mix together. Add APSand TEMED just before pouring.	.	.

10% APS	25ul	25ul
TEMED	5ul	5ul
.	5ml	5ml

Preparations of sample: Protein samples are in 1X sample loading buffer (also called Laemmli dye)...ie to 6 ul protein sample, add 3 ul 3X Laemmli dye stock. Boil 3 minutes before loading gel.

Sample loading buffer (Laemmli loading dye) 3X stock:
1M Tris-Cl pH 6.8 2.4 ml
20% SDS 3 ml
Glycerol (100%) 3 ml
B-mercaptoethanol 1.6 ml
Bromophenol blue 0.006g
10 ml (store 4℃)


For BioRad apparatus: need 500 ml of 1X buffer so dilute 50 ml 10X stock + 450 ml dH₂O
Running gels: Using the BioRad apparatus, run gels at 200V (constant voltage) until the bromophenol blue dye is just off. Takes 50-60 minutes. Gels are run at room temperature.