ULB/5 September 2009

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<li><a class="mainlink" href="/Team:ULB-Brussels/Project">Project</a></li>
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<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 10:26, 21 October 2009

iGEM Team:ULB-Brussels Wiki


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Positive results for bacterial transformations performed on 9/4. Extraction and migration of plasmids with following genes:

  • 1st well: LuxPr (R0062)
  • 2nd well: P0152
  • 3th well: cl 434 (R0052)
  • 4th well: promoter repressed by cIIp22 and activated by HSL-LuxR (K14150)
  • 5th well: cII p22 (R0053)
  • 6th well: GFP (e0240)
  • 7th well: luxR (I0462)

=> Results (see below): negative for: luxPr (R0062), P0152, K14150, cII p22 (R0053), others are positive.

5 9.jpg

Ligation:

Insert Plasmid
1


2
3
4 LuxpR
5