INSA-Lyon/30 September 2010

From 2010.igem.org

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<p>(mise en collection) of I0500, 10L and 4O </p><br>
<p>(mise en collection) of I0500, 10L and 4O </p><br>
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<p>Agarose gel electrophoris : <br>
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<p>Agarose gel electrophoresis : <br>
<ol id="list_extra">
<ol id="list_extra">
<li>8C/14K :ok (mise en collection)</li>
<li>8C/14K :ok (mise en collection)</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>
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</ol><br></p>
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<p>Agarose gel electrophoris for purification : we can't see anything so we will do it again later</p><br>
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<p>Agarose gel electrophoresis for purification : we can't see anything so we will do it again later</p><br>
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<p>DNA extraction, digestion with E and agarose gel electrophoris for the 10 clones of 1F/24A/14K : the higher weigh were not separated, to do again</p>
+
<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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Revision as of 12:30, 8 October 2010





September 30th


(mise en collection) of I0500, 10L and 4O


Agarose gel electrophoresis :

  1. 8C/14K :ok (mise en collection)
  2. 8C : nothing (!?)
  3. pha B : OK, purification of the band

Digestion :

  1. 18A, phaA : with E+S
  2. 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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