Basic Protein Chemistry Techniques

Coomassie Blue Stain:  (for gels)
1) Combine 225 ml Methanol with 225 ml ddH2 O.
2) Add 0.5 grams of Coomassie Blue.
3) Just before use, add 50 ml acetic acid to 10% final concentration.
4) Stain for 2 hours. Staining time can be shortened by microwaving; ~50 seconds at medium power.
5) After staining, pour off the stain into a bottle marked Used Stain.  Stain can be re-used once, but fresh 10% acetic acid must be added).


Coomassie Blue Destain:  (for gels)
1) Combine 25 ml of Methanol with 437.5 ml ddH2 O.
2) Just before use, add 37.5 ml acetic acid to 7.5% final concentration.
3) Destain, plus sponges (pieces of foam packing) for a couple of hours.  It may be necessary to use more than one change of destain.   Microwaving can be used in this stage also, but the details have not been determined.

 
Coomassie Blue Stain:  (for membranes)
1) Combine 50 ml of Methanol with 50 ml of ddH2 O.
2) Add 0.1 g of Coomassie Blue.
3) Stain by pouring a sufficient amount to cover the membrane in a petri dish.
4) Wash the fluid gentle back and forth over the membrane.  Allow it to be immersed for one to two minutes.
5) Dispose of stain in a manner similar to that for the gel stain.

Dialysis Tubing Prep
1) Cut tubing to appropriate lengths and place them in a large beaker.
2) Add enough 5% NaHCO₃ (add 50 grams per liter of ddH2 O) to cover the tubing.
3) Bring to a rolling boil and allow it to boil for 15 minutes.  The tubing will float so place a beaker of the next smaller size on top of the tubing.
4) Rinse the tubing with an excess of ddH2 O.
5) Soak the tubing in 2 mM EDTA (add 10 ml 0.2 M to 1 liter ddH2 O) for one hour.
6) Rinse again with an excess of ddH2 O.
7) Store in 0.05% Azide (add 0.005 ml per liter of ddH2 O).

To Pour Stacking Gel...
0.4mls  Acrylamide                   
0.4mls  10x Stacking Buffer       
40uls  10% SDS   
3.12mls  ddH2 0   
2uls  Temed   
34uls  APS   

How to Make 15% Mini-gels