Team:UIUC-Illinois/Notebook/Protocols/GelElectrophoresis
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- | <center><h1> | + | <center><h1>Making Gel Electrophoresis gel solutions</h1></center> <br/><br/> |
+ | |||
+ | <h2>To check PCR results</h2><br/> | ||
+ | |||
+ | What you need:<br/><br/> | ||
+ | - High-melt agarose<br/> | ||
+ | - TAE buffer 1X<br/> | ||
+ | - Autoclaved container <br/><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/> | ||
+ | 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/> | ||
+ | 3. BE CAREFUL AS LIQUID CAN BE SUPERHEATED<br/><br/> | ||
+ | |||
+ | <h2>To do a gel purification</h2><br/> | ||
+ | What you need:<br/><br/> | ||
+ | - Low-melt agarose<br/> | ||
+ | - TAE buffer 1X<br/> | ||
+ | - Autoclaved container <br/><br/> | ||
+ | Procedure:<br/><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/> | ||
+ | 3. BE CAREFUL AS LIQUID CAN BE SUPERHEATED<br/><br/> | ||
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+ | |||
+ | |||
</div> | </div> | ||
Latest revision as of 15:32, 4 June 2012