Team:Groningen/protocols/GelElectrophoresis
From 2013.igem.org
(Difference between revisions)
Line 22: | Line 22: | ||
<div class="mainContent"> | <div class="mainContent"> | ||
- | + | <h1>Gel electrophoresis</h1> | |
+ | |||
+ | <h3>Materials:</h3> | ||
+ | <ul type="square"> | ||
+ | <li></li> | ||
+ | <li></li> | ||
+ | <li></li> | ||
+ | <li></li> | ||
+ | <li></li> | ||
+ | </ul> | ||
+ | |||
+ | <h3>:</h3> | ||
+ | |||
+ | <br>All the reagents are added following the order listed in the table above. | ||
+ | <br>After the reaction is ready mix the content of the tube and spin it down. | ||
+ | <br>The tubes are incubated for 1h at 37°C. | ||
+ | <br> | ||
+ | <br>Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/fast-digestion-dna.pdf | ||
</div> | </div> |
Revision as of 10:34, 26 July 2013
Gel electrophoresis
Materials:
:
All the reagents are added following the order listed in the table above.
After the reaction is ready mix the content of the tube and spin it down.
The tubes are incubated for 1h at 37°C.
Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/fast-digestion-dna.pdf