Team:UPO-Sevilla/Notebook/09 10

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       <h2>Assay Team</h2>
       <h2>Assay Team</h2>
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       <p>We develop different assays by changing different features; the plates are incubated overnight.</p>
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       <p>We developed different assays by changing different features; the plates were incubated overnight.</p>
     <a class="return_button" href="/Team:UPO-Sevilla/Notebook/09_09" title="Go to 9th of September"><span>Go to 9th of September</span></a>
     <a class="return_button" href="/Team:UPO-Sevilla/Notebook/09_09" title="Go to 9th of September"><span>Go to 9th of September</span></a>

Latest revision as of 20:59, 26 October 2010

September, 10th

Production Team

We changed some conditions to improve our PCR results:

  • We used new Pfu enzyme, buffer and dNTP.
  • Templates: we diluted the high concentrated fragment (1/10) and used 2ul instead of 1ul of the low concentrated one.

0’8% gel electrophoresis analysis showed a line of 1Kb, which is the length of fecR. There was also a 0’2Kb line. It looked like that the new conditions carried us to the goal. We had to isolate from gel the new part: WE GOT FECR!

Assembly Team

We realized a new ligation of the failed biobricks and digested not available biobricks (2+6) and vectors (pSB1C3 and pSB1T3).

Assay Team

We developed different assays by changing different features; the plates were incubated overnight.

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