Team:Grenoble/Biology/Protocols/Gel
From 2012.igem.org
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<h2>Run the gel</h2> | <h2>Run the gel</h2> | ||
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- | <li> | + | <li>Connect the generator.</li> |
+ | <li>Chose the right voltage.</li> | ||
+ | <li>Put the device on.</li> | ||
</div> | </div> | ||
Revision as of 09:05, 28 August 2012
Gel electrophoresis
Goal
Separate DNA strands of different lengths.Prepare the gel
- Add 1 g of agarose powder to 50 mL of 1X TAE buffer.
- Heat the solution using the microwave until the powder is completely dissolved.
- Once the solution is cool enough to be touched, pour it into gel cast (don't forget the comb).
Load the gel
- When the gel is solid, remove carefully the comb.
- Place the gel in the buffer tank and cover it with the 1X TAE buffer solution.
- Load each sample into the wells (don't forget the loading dye and the DNA ladder).
Run the gel
- Connect the generator.
- Chose the right voltage.
- Put the device on.