Team:Groningen/protocols/GelElectrophoresis
From 2013.igem.org
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- | <h5>Procedure:</h5> | + | <p><h5>Procedure:</h5> |
- Mix the DNA samples in a 1:1 ratio with 2x Loading Dye | - Mix the DNA samples in a 1:1 ratio with 2x Loading Dye | ||
<br>- Load the samples on gel | <br>- Load the samples on gel |
Revision as of 10:35, 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.