Difference between revisions of "Team:UiOslo Norway/Experiments/SDS-Page"
Line 33: | Line 33: | ||
<table id="t01"> | <table id="t01"> | ||
<tr> | <tr> | ||
− | <th | + | <th>12 % </th> |
− | <th | + | <th>18 % </th> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>2 ml</td> |
− | <td | + | <td>2 ml</td> |
− | <td | + | <td>Seperating buffer (1.5 M Tris pH 8.8)</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>3.2 ml</td> |
− | <td | + | <td>4.8 ml</td> |
− | <td | + | <td>30 % Acrylamide (37.5:1)</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>2.7 ml</td> |
− | <td | + | <td>1.1 ml </td> |
− | <td | + | <td>Water</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>80 μl</td> |
− | <td | + | <td>80 μl</td> |
− | <td | + | <td>10% (w/v) SDS</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>8 μl</td> |
− | <td | + | <td>8 μl</td> |
− | <td | + | <td>TEMED</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td | + | <td>80 μl</td> |
− | <td | + | <td>80 μl</td> |
− | <td | + | <td>APS</td> |
</tr> | </tr> | ||
Revision as of 12:09, 14 August 2015
SDS-Page:
Back to ProtocolsReagent
Stacking Gel: 0.7 ml 30 % Acrylamide (37.5:1) 1.25 ml Stacking gel buffer (1 M Tris pH 6.8) 3 ml Water 50 ul 10 % (w/v) SDS 5 ul TEMED 50 ul APS
Separating gel:
12 % 18 % 2 ml 2 ml Seperating buffer (1.5 M Tris pH 8.8) 3.2 ml 4.8 ml 30 % Acrylamide (37.5:1) 2.7 ml 1.1 ml Water 80 μl 80 μl 10% (w/v) SDS 8 μl 8 μl TEMED 80 μl 80 μl APS Run SDS-Page for 1 hour at 30 mA per gel
Coomassie-staining
Quick Coomassie staining solution: 1 % (w/v) Coomassie Brilliant Blue R250 50 % (v/v) Methanol 10 % (v/v) Acetic acid Coomassie Destaining solution: 40 % (v/v) Methanol 10 % (v/v) Acetic acid