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

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       <td>Participants:</td>
 
       <td>Participants:</td>
       <td>Dominic</td>
+
       <td>Dominic Schwarz</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td>Protocol:</td>
 
       <td>Protocol:</td>
       <td>epo. Trafo</td>
+
       <td>
 +
<a href="https://static.igem.org/mediawiki/2018/c/ca/T--Munich--WL1_Electrocompetent_transformation.pdf" target="_blank">Electrocompetent transformation</a>
 +
</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
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       <td>Participants:</td>
 
       <td>Participants:</td>
       <td>Eni</td>
+
       <td>Enikö Baligács</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td>Protocol:</td>
 
       <td>Protocol:</td>
       <td>PCR, agarose gel, gelextraction</td>
+
       <td>
 +
<a href="https://static.igem.org/mediawiki/2018/3/3c/T--Munich--WL1_PCR.pdf" target="_blank">PCR</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/b/be/T--Munich--WL1_Agarose-Gel_electrophoresis.pdf" target="_blank">Agarose gel</a>,  
 +
<a href="https://international.neb.com/protocols/2015/11/23/monarch-dna-gel-extraction-kit-protocol-t1020" target="_blank">Gel extraction</a>
 +
</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>

Revision as of 20:08, 15 October 2018

Transforming E. Coli DH5a to amplify pKD3 for pRED/ET engineering

2018/05/28
Participants: Dominic Schwarz
Protocol: Electrocompetent transformation
Notes: we also inoculated LB media blindly.
Results: no colonies, no growth;
We decided to use a resistance cassette from pSB1C3 without FRT sites

Amplifying a selection cassette from pSB1C3

2018/05/29
Participants: Enikö Baligács
Protocol: PCR, Agarose gel, Gel extraction
Notes: Primer with 50bp homology regions ????, TA: 67°C, Elongation: 45s
Results: PIC. we thought the band might be what we wanted but because of how few DNA the extraction yielded, these samples were not used in further experiments.