Team:Groningen/protocols/GelElectrophoresis
From 2013.igem.org
(Difference between revisions)
Line 35: | Line 35: | ||
<h5>Procedure:</h5> | <h5>Procedure:</h5> | ||
+ | - Mix the DNA samples in a 1:1 ratio with 2x Loading Dye | ||
+ | - Load the samples on gel | ||
+ | - Load the 1kb GeneRuler of Fermentas on gel | ||
+ | - Run the gel at 90V for 24-45 minutes to separate the bands. | ||
+ | |||
All the DNA samples are mixed 1:1 ratio with Loading Dye 2x. | All the DNA samples are mixed 1:1 ratio with Loading Dye 2x. | ||
<br>The samples are loaded on a 0.8% or 1.5% agarose gel (diluted in TBE buffer 1x), with next to it a DNA 1kb GeneRuler of Fermentas. | <br>The samples are loaded on a 0.8% or 1.5% agarose gel (diluted in TBE buffer 1x), with next to it a DNA 1kb GeneRuler of Fermentas. |
Revision as of 10:32, 28 July 2013
Gel electrophoresis
Materials:
- Power supply
- 0.8 or 1.5% agarose gel
- Gel tray
- 2x Loading Dye
- DNA samples
- DNA 1kb GeneRuler of Fermentas
Procedure:
- Mix the DNA samples in a 1:1 ratio with 2x Loading Dye - Load the samples on gel - Load the 1kb GeneRuler of Fermentas on gel - Run the gel at 90V for 24-45 minutes to separate the bands. All the DNA samples are mixed 1:1 ratio with Loading Dye 2x.The samples are loaded on a 0.8% or 1.5% agarose gel (diluted in TBE buffer 1x), with next to it a DNA 1kb GeneRuler of Fermentas.
The gel is placed in TBE buffer 1x and a 90V electric potential is applied to the gel for 24-45 minutes to seperate the bands.