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ULB/24 July 2009
From 2009.igem.org
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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> |
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<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 10:47, 21 October 2009
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No pertinent result emerged from the gradient PCR.
RBS primers hybridisation
A restriction digest was performed to cut the plasmid with EcoRI and XhoI.
PCR (deletion program) on hfsH gene at 68°C with and without DMSO (the mix has been 10 times diluted).
hfsH and hfsG genes have been ordered for the assembly standard 10.
