Team:EPF-Lausanne/Protocol/Silver staining

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[[File:Team-EPF-Lausanne_ssp.jpg|470px]]
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*Loading Plan
 
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*Lane 1: Ladder
 
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*Lane 2: Empty well
 
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*Lane 3: 10microL of VP16 only
 
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*Lane 4: 25microL of VP16 only
 
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*Lane 5: Nontransfected CHO cell - High concentration (5million)
 
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*Lane 6: Sample 1 48h of expression
 
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*Lane 7: Sample 2 48h of expression
 
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*Lane 8: Sample 1 72h of expression
 
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*Lane 9: Sample 2 72h of expression
 
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*Lane 10: Nontransfected CHO cell - Same concentration as samples
 
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[[File:Team-EPF-Lausanne_21.sep.12 ssr.jpg|600px]]
 
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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 16:08, 26 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