Difference between revisions of "Team:KAIT Japan/Protocol"
Line 127: | Line 127: | ||
7) Dye the gel with CBB for 30 minutes<br> | 7) Dye the gel with CBB for 30 minutes<br> | ||
8) Branch the gel for 2 hours while shaking it<br> | 8) Branch the gel for 2 hours while shaking it<br> | ||
+ | <br> | ||
+ | <img src="https://static.igem.org/mediawiki/2015/b/bf/Geru1.PNG"><br> | ||
<br> | <br> | ||
<img src=""> | <img src=""> |
Revision as of 07:18, 18 September 2015
Protocol
[SDS-PAGE]
1) Prepare the gel
2) Place stacking gel on separating gel
3) Fill electrophoresis chamber electrophoretic buffer
4) Add 4×sample buffer the cooldshock expressed protein sample and heat block (95℃,10minutes)
5) Load prepared sample into wells
6) Run the electrophoresis in 15mA, 1 hour 25 minutes
7) Dye the gel with CBB for 30 minutes
8) Branch the gel for 2 hours while shaking it