Difference between revisions of "Team:Munich/engineering2.html"

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     <tr>
 
     <tr>
 
       <td>Notes:</td>
 
       <td>Notes:</td>
       <td>MG1655 is E.Coli WT as backup
+
       <td>Genetic engineering is planned in E. Coli Rosetta, MG1655 is E.Coli WT as backup.
 
</td>
 
</td>
 
     </tr>
 
     </tr>
 
  <tr>
 
  <tr>
 
       <td>Results:</td>
 
       <td>Results:</td>
       <td>colonies only on MG1655 plate
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       <td>colonies only on E. Coli MG1655 plate;
No colonies on E.coli Rosetta
+
No colonies on E. Coli Rosetta
 
</td>
 
</td>
 
     </tr>
 
     </tr>
 
</table>
 
</table>
  
 
<h3>8/29</h3>
 
 
<h4>pRED/ET genome engineering of delta msb-B and delta recBCD strains</h4>
 
<h4>pRED/ET genome engineering of delta msb-B and delta recBCD strains</h4>
 +
<em>2018/08/29</em>
 
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       <td>Results:</td>
 
       <td>Results:</td>
       <td>red colonies
+
       <td>red colonies. Elena (Advisor) and Dominic decided to repeat the experiment but to do a dpnI digest before to get rid of the template DNA.
Redoing the experiment but doing a dpni digest before
+
 
+
 
</td>
 
</td>
 
     </tr>
 
     </tr>
 
</table>
 
</table>
  
<h3>8/30</h3>
 
 
<h4>Transforming E. Coli DH5a to find a reason for the contamination</h4>
 
<h4>Transforming E. Coli DH5a to find a reason for the contamination</h4>
 +
<em>2018/08/30</em>
 
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Revision as of 15:14, 29 September 2018

Transforming E. Coli Rosetta and MG1655 for pRED/ET engineering

2018/08/28

Participants: Dominic
Protocol: epo trafo
Notes: Genetic engineering is planned in E. Coli Rosetta, MG1655 is E.Coli WT as backup.
Results: colonies only on E. Coli MG1655 plate;

No colonies on E. Coli Rosetta

pRED/ET genome engineering of delta msb-B and delta recBCD strains

2018/08/29

Participants: Dominic
Protocol: pRED/ET engineering protocol
Notes: the template for the resistance cassette for deletions was taken from a plasmid containing mRFP
Results: red colonies. Elena (Advisor) and Dominic decided to repeat the experiment but to do a dpnI digest before to get rid of the template DNA.

Transforming E. Coli DH5a to find a reason for the contamination

2018/08/30

Participants: Dominic
Protocol: epo trafo
Notes: CAP_recBCD, CAP_msbb, psb1c3_mrfp in Dh5a
Results: red colonies on all plates -> mRFP contamination