INSA-Lyon/30 September 2010
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- | <p> | + | <p>Genomic library of I0500, 10L and 4O </p><br> |
- | <p>Agarose gel | + | <p>Agarose gel electrophoresis : <br> |
<ol id="list_extra"> | <ol id="list_extra"> | ||
- | <li>8C/14K :ok | + | <li>8C/14K :ok ->Genomic library</li> |
<li>8C : nothing (!?)</li> | <li>8C : nothing (!?)</li> | ||
<li>pha B : OK, purification of the band</li> | <li>pha B : OK, purification of the band</li> | ||
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<li>14/12/13, pha B and L2/1N : with X+P</li> | <li>14/12/13, pha B and L2/1N : with X+P</li> | ||
</ol><br></p> | </ol><br></p> | ||
- | <p>Agarose gel | + | <p>Agarose gel electrophoresis for purification : we can't see anything so we will do it again later</p><br> |
- | <p>DNA extraction, digestion with E and agarose gel electrophoris for the 10 clones of 1F/24A/14K : the higher | + | <p>DNA extraction, digestion with E and agarose gel electrophoris for the 10 clones of 1F/24A/14K : the higher weights were not separated, to do again</p><br><br> |
+ | <p>Gel verification for plasmid backbones PCR (about 0,7%): nothing on the gel!! Maybe, PCR on the plasmid is better.</p><br> | ||
+ | <p>From transformation negative control, we purified XL-Blue Cells on GL, at 37°C overnight.</p><br> | ||
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Latest revision as of 20:10, 25 October 2010
September 30th
Genomic library of I0500, 10L and 4O
Agarose gel electrophoresis :
- 8C/14K :ok ->Genomic library
- 8C : nothing (!?)
- pha B : OK, purification of the band
Digestion :
- 18A, phaA : with E+S
- 14/12/13, pha B and L2/1N : with X+P
Agarose gel electrophoresis for purification : we can't see anything so we will do it again later
DNA extraction, digestion with E and agarose gel electrophoris for the 10 clones of 1F/24A/14K : the higher weights were not separated, to do again
Gel verification for plasmid backbones PCR (about 0,7%): nothing on the gel!! Maybe, PCR on the plasmid is better.
From transformation negative control, we purified XL-Blue Cells on GL, at 37°C overnight.
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