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Team:Newcastle/Gel electrophoresis
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RachelBoyd (Talk | contribs)
(New page: {{Team:Newcastle/mainbanner}} ===Gel electrophoresis=== *Transfer harden gel into the gel tank *add TAE buffer until the gel is completely submerged *Depending on the nature of the samp...)
Newer edit →
(New page: {{Team:Newcastle/mainbanner}} ===Gel electrophoresis=== *Transfer harden gel into the gel tank *add TAE buffer until the gel is completely submerged *Depending on the nature of the samp...)
Newer edit →
Revision as of 09:41, 27 July 2010
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Gel electrophoresis
- Transfer harden gel into the gel tank
- add TAE buffer until the gel is completely submerged
- Depending on the nature of the sample, 3μl of GeneRuler™ 1kb Plus DNA Ladder
- Loading buffer was then added together with the sample before loading onto the gel matrix
- Run gel at 90V until separation is achieved and visualize using the gelDoc
