移液器

BASICNATIVE GEL Protocol

Stock Solutions
1) 1.5M TrisHCl pH 8.9 - Keep RT. 2) 30% Acrylamide 0.8% Methylene bis Acrylamide. Keep 4°C. 3) 0.5M TrisHCl pH 6.8 - Keep RT. 4) 10% Ammonium Persulfate (APS). Keep 4°C less than 1 month.
Running Buffer x1
Trizma
0.05M
1.21gr
Glycine
0.38M
5.32gr
H2O up to
200ml
Adjust pH to
8.9
Keep at RT
Dissolving Buffer x5
Glycerol
5ml
H2O
2.7ml
0.5M TrisHCl pH 6.8
2.13ml
Bromo Phenol Blue
traces

Keep in aliquots of 1ml at -20C

Separating Gel
% Acrylamide
10%
10%
12%
12%
15%
Number of Minigels
5
8
5
8
5
1.5M TrisHCl pH 8.9
7.0 ml
10.5 ml
7.0 ml
10.5 ml
7.0 ml
30% Acrylamide 0.8% Methylene bis Acrylamide
9.3 ml
13.9 ml
11.3 ml
16.9 ml
13.9 ml
H2O
12.3 ml
18.4 ml
9.3 ml
13.9 ml
6.3 ml
10% APS
100 ul
150 ul
100 ul
150 ul
100 ul
TEMED
23 ul
35 ul
23 ul
35 ul
23 ul

Add TEMED and APS at the end. Gently swirl the flask to mix, being careful not to generate bubbles. Pipette the solution to a level of 4cm of the top. Add 0.3ml of n-buthanol. A very sharp liquid interface will be visible within 10-20min. Let polymerize the gel for another hour at least. Rinse the surface of the gel with H2O before pouring the stacking gel.

Stacking Gel

Number of Minigels
2
5
8
0.5M TrisHCl pH 6.8
2.5 ml
4.0 ml
5.2 ml
30% Acrylamide 0.8% Methylene bis Acrylamide
1.0 ml
1.5 ml
2.0 ml
H2O
6.4 ml
9.6 ml
12.8 ml
10% APS
100 ul
150 ul
200 ul
TEMED
10 ul
15 ul
20 ul

Fill each sandwich with stacking gel solution and insert a comb into each place taking care not to trap any bubbles bellow the teeth. The gel should fully polymerized after 1hour. Cover gel with a wrap nylon. Keep gel at 4C no more than 2 days; use only fresh gels. Running conditions: 30mA / 250V max.

Sample Preparation

Prior to adding the sample buffer, keep samples at 0°C. Add the sample buffer (RT) to the sample (still on ice), and load immediately. For a gel thickness of 0.75mm and 15 wells applied 0.5 to 5ug for Coomasie Blue stain and 10 to 100-fold less protein for silver stain. If you do not know the electrophoretic pattern of your protein, load same sample in parallel wells at different times during the run. Use only purified or paritally purified material.

Staining Solution

Methanol CP
500ml
50%
Acetic Acid CP
100ml
10%
H2O
400ml
Coomasie Brilliant Blue R
2.5gr
0.25%

Keep flask on dark at RT

Destaining Solution

Methanol CP
150ml
15%
Acetic Acid CP
100ml
10%
H2O
750ml

Keep flask on dark at RT

Stain overnight at RT or put gel with staining solution few seconds in microwave on the high position, and then shake for another 15min at RT. Wash with water 2-3 times and distain by several changes of destaining solution in the presence of a sponge.

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