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Team:Paris/July 29
From 2008.igem.org
(New page: ==Digestion of DNA== for each reaction (total volume : 50 µL) * 20 µL of DNA (MiniPrep product) * 2 µL of enzyme 1 * 2 µL of enzyme 2 * 5 µL of buffer 2 (10X) * 20,5 µL water Each ...)
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Revision as of 10:40, 30 July 2008
Digestion of DNA
for each reaction (total volume : 50 µL)
- 20 µL of DNA (MiniPrep product)
- 2 µL of enzyme 1
- 2 µL of enzyme 2
- 5 µL of buffer 2 (10X)
- 20,5 µL water
Each reaction was incubated 2 hours at 37°C, then 10 minutes at 60-65°C (to inactivate the enzymes). 10 µL of loading dye (6X) were added to each of the 50 µL of digestion product. The whole samples were run in a 1,5% agarose gel (about 30 minutes at 100 W ; 2 x 30 µL per sample ; 30 µL per well). The bands of interest were then excised from the gel and the DNA was purified using the QIAquick DNA Gel Extraction kit (QIAGEN). Unfortunately, there were not enough columms, so we took some columms from the QIAGEN MiniPrep kit, hoping that it will work with the QIAquick DNA Gel Extraction kit. Some of the samples were too voluminous, so we separated them into two tubes. The elution of DNA was performed using 50 µL of water (after 10 minutes of incubation at 37°C).
Each of the samples was then analysed by a 1,5% agarose gel:
- 2 µL of DNA
- 3 µL of water
- 1 µL of 6X loading dye
The ladder used was the 100 bp ladder from New England Biolabs.
