Team:UPO-Sevilla/Notebook/09 08

From 2010.igem.org

(Difference between revisions)
(New page: <div class=globalBC> {{:Team:UPO-Sevilla/header}} <!-- --> <html> <head> <script type="text/javascript" language="javascript"> <!-- current("notebook","http...)
Line 26: Line 26:
       <p>Transformation of <i>E. coli</i> DH5-alfa with the products of ligations, and we spread in selective plates.</p>
       <p>Transformation of <i>E. coli</i> DH5-alfa with the products of ligations, and we spread in selective plates.</p>
-
 
+
 
 +
      <h2>Assay Team</h2>
 +
 
 +
      <p>We carried out the assay without any problem but we must wait to see the results. We have to incubate the plates overnight.</p> 
 +
 
     <a class="return_button" href="/Team:UPO-Sevilla/Notebook" title="Notebook"><span>Return to Notebook</span></a>
     <a class="return_button" href="/Team:UPO-Sevilla/Notebook" title="Notebook"><span>Return to Notebook</span></a>

Revision as of 16:59, 17 October 2010

September, 08th

Production Team

David Caballero. We performed the second overlapping PCR reaction of the SDM with the former and purified PCR products. We carried out two strategies: in one PCR reaction we used the original concentration and in another we used a 1/10 dilution of it.

Products of these PCR reactions were analyzed in 0,8% gel electrophoresis and it was shown that there were not amplification.

Assembly Team

Transformation of E. coli DH5-alfa with the products of ligations, and we spread in selective plates.

Assay Team

We carried out the assay without any problem but we must wait to see the results. We have to incubate the plates overnight.

Return to Notebook

Footer