ULB/9 September 2009

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<li><a class="mainlink" href="/Team:ULB-Brussels/Project">Project</a></li>
<li><a class="mainlink" href="/Team:ULB-Brussels/Project">Project</a></li>
<li><a class="mainlink" href="/Team:ULB-Brussels/Parts">Parts</a></li>
<li><a class="mainlink" href="/Team:ULB-Brussels/Parts">Parts</a></li>
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<li><a class="mainlink" href="/Team:ULB-Brussels/Modeling">Modeling</a></li>
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<li><a class="mainlink" href="/Team:ULB-Brussels/Safety">Safety</a></li>
<li><a class="mainlink selection" href="/Team:ULB-Brussels/Notebook">Notebook</a></li>
<li><a class="mainlink selection" href="/Team:ULB-Brussels/Notebook">Notebook</a></li>
<li><a class="mainlink" href="/Team:ULB-Brussels/Sponsors">Sponsors</a></li>
<li><a class="mainlink" href="/Team:ULB-Brussels/Sponsors">Sponsors</a></li>

Latest revision as of 10:25, 21 October 2009

iGEM Team:ULB-Brussels Wiki


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  • Plasmid extraction of 5 ligations : concentrations obtained by photometry at around 20 ng. The gel migration of ligations has failed.
  • we have migrated digestion of plasmids containing the construction glue : Results : No band appears again .
  • The transformations of the tube 4 to tube 5 were transplanted.
  • The transformations of the tube 10 with the tube 9 have given nothing and we started this ligation Called lig B
  • We have league 1 with the ligation ligation 2 (the first 2 buildings of the circuit). we called lig A.
  • We cast boxes with a gradient of aspartate in order to observe chemotactism of bacterium.