Team:EPF-Lausanne/Protocol/Silver Staining

From 2012.igem.org

(Difference between revisions)
Line 86: Line 86:
[[File:Team-EPF-Lausanne_ssp.jpg|470px]]
[[File:Team-EPF-Lausanne_ssp.jpg|470px]]
 +
[[File:Team-EPF-Lausanne_21.sep.12 ssr.jpg|600px]]
 +
 +
Result: The lane 9 (Lovtap-VP16 transfected CHO cell) and lane 10 (non-transfected CHO cell) have intensity difference around 30~35kDa area.

Revision as of 23:18, 23 September 2012

Protocol: Silver Staining

Gel making

Gel Ingredients (choose percentage according to the size of the protein)

4-40 kDA 20%
12-45 kDA 15%
10-70 kDA 12.5%
15-100 kDA 10%
25-200 kDA 8%


Separating gel
Gel percentage 7.5 %
30% Polyacrylamide 10 mL
1.5M Tris (pH 8.8) 10 mL
10% Ammonium persulfate 0.4 mL
10% SDS 0.4 mL
TEMED 0.038 mL
H2O 19.2 mL
Total volume 40 mL
Stacking gel
Gel percentage 5 %
30% Polyacrylamide 1.36 mL
1M Tris (pH 6.8) 1 mL
10% Ammonium persulfate 0.08 mL
10% SDS 0.08 mL
TEMED 0.008 mL
H2O 5.44 mL
Total volume 8 mL


Team-EPF-Lausanne ssp.jpg Team-EPF-Lausanne 21.sep.12 ssr.jpg

Result: The lane 9 (Lovtap-VP16 transfected CHO cell) and lane 10 (non-transfected CHO cell) have intensity difference around 30~35kDa area.