Team:UIUC-Illinois/Notebook/Protocols/GelElectrophoresis
From 2012.igem.org
(Difference between revisions)
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- Autoclaved container <br/><br/> | - Autoclaved container <br/><br/> | ||
- | Procedure:<br/> | + | Procedure:<br/><br/> |
1. Add 3.2g high-melt agarose to 400 mL 1X TAE buffer (50 uL agarose gel, 250 mL 1X TAE buffer for the small gel box) <br/> | 1. Add 3.2g high-melt agarose to 400 mL 1X TAE buffer (50 uL agarose gel, 250 mL 1X TAE buffer for the small gel box) <br/> | ||
2. Microwave flask or bottle (cap placed loosely if bottle) of mixed solution to dissolve gel in 1 minute increments until all agarose is dissolved<br/> | 2. Microwave flask or bottle (cap placed loosely if bottle) of mixed solution to dissolve gel in 1 minute increments until all agarose is dissolved<br/> | ||
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- TAE buffer 1X<br/> | - TAE buffer 1X<br/> | ||
- Autoclaved container <br/><br/> | - Autoclaved container <br/><br/> | ||
- | Procedure:<br/> | + | Procedure:<br/><br/> |
1. Add 4.0g low-melt agarose to 400 mL 1X TAE buffer<br/> | 1. Add 4.0g low-melt agarose to 400 mL 1X TAE buffer<br/> | ||
2. Microwave flask or bottle (cap placed loosely if bottle) of mixed solution to dissolve gel in 1 minute increments until all agarose is dissolved<br/> | 2. Microwave flask or bottle (cap placed loosely if bottle) of mixed solution to dissolve gel in 1 minute increments until all agarose is dissolved<br/> |
Revision as of 19:50, 1 June 2012