ULB/4 August 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> | ||
- | <li><a class="mainlink" href="/Team:ULB-Brussels/ | + | <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 10:46, 21 October 2009
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laboratory manipulation
Purification of hfsG.
Analysis of hFSH: we notice that the primers can bind to 25 different locations in the genome of Caulobacter. We will digest the genome with a maximum of possible sites to better identify the hFSH (selection of a restriction enzymes which don't cut hFSH) before doing a PCR with "Blunt" primers.