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 | + | <br>- Mix the DNA samples in a 1:1 ratio with 2x Loading Dye |
- | - Load the samples on gel | + | <br>- Load the samples on gel |
- | - Load the 1kb GeneRuler of Fermentas on gel | + | <br>- Load the 1kb GeneRuler of Fermentas on gel |
- | - Run the gel at 90V for 24-45 minutes to separate the bands. | + | <br>- 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. |
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.