Difference between revisions of "Team:Munich/chibiobrick1.html"

 
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<div class="event-info">
 
<div class="event-info">
  
<p>2018/06/04<p>
+
 
 +
<h4>Forming Oligodimers from Single-Strand DNA chi6 Sequences</h4>
 +
<em>2018/06/01</em>
 +
<table class="table table-borderless">
 +
    <tr>
 +
 
 +
      <td>Participants:</td>
 +
      <td>Dominic Schwarz</td>
 +
    </tr>
 +
    <tr>
 +
      <td>Protocol:</td>
 +
      <td><a href="https://www.sigmaaldrich.com/technical-documents/protocols/biology/annealing-oligos.html" target="_blank">Oligodimerization</a>
 +
</td>
 +
</tr>
 +
<tr>
 +
      <td>Notes:</td>
 +
      <td> Oligodimers were bought
 +
</td>
 +
    </tr>
 +
 
 +
    </tr>
 +
</table>
 +
 
 +
 
 
<h4>Assembling pSB1C3_Chi6 with A3 Assembly</h4>
 
<h4>Assembling pSB1C3_Chi6 with A3 Assembly</h4>
 +
<em>2018/06/04</em>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>
  
 
       <td>Participants:</td>
 
       <td>Participants:</td>
       <td>Dominic</td>
+
       <td>Dominic Schwarz</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
       <td>Protocols:</td>
+
       <td>Protocol:</td>
       <td>restriction digest, Ligation, chem trafo, mini-prep, sequencing</td>
+
       <td>
 +
<a href="https://static.igem.org/mediawiki/2018/7/7e/T--Munich--WL1_Restriction_Digest.pdf" target="_blank">Restriction digest</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/1/1a/T--Munich--WL1_Ligation.pdf" target="_blank">Ligation</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/a/a5/T--Munich--WL1_Chemical_transformation.pdf" target="_blank">Chemical transformation</a>,  
 +
<a href="https://international.neb.com/protocols/2015/11/20/monarch-plasmid-dna-miniprep-kit-protocol-t1010" target="_blank">Miniprep</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/a/ab/T--Munich--WL1_Sequencing_sample_preparation.pdf" target="_blank">Sequencing</a>
 +
 
 +
 
 +
</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td>Notes:</td>
 
       <td>Notes:</td>
       <td> digest with XbaI, SpeI <br>
+
       <td>pSB1C3 Backbone was generated by restriction with XbaI and SpeI. Chi6 Dimers were digested with XbaI & SpeI.<br>
transformation of Dh5a
+
Transformation of Dh5a
 
</td>
 
</td>
 
     </tr>
 
     </tr>
 
  <tr>
 
  <tr>
       <td>Results:</td>
+
       <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td>
       <td>no sequence obtained for the given primers. The samples must be contaminated. We decided to redo the experiment.</td>
+
       <td>No sequence obtained for the given primers. The samples must be contaminated. We decided to redo the experiment.</td>
 
     </tr>
 
     </tr>
 
</table>
 
</table>
  
<p>2018/06/06 - 2018/06/26<p>
+
 
 
<h4>Redo: Assembling pSB1C3_Chi6 with A3 Assembly</h4>
 
<h4>Redo: Assembling pSB1C3_Chi6 with A3 Assembly</h4>
 +
<em>2018/06/06 - 2018/06/26</em>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>
  
 
       <td>Participants:</td>
 
       <td>Participants:</td>
       <td>Dominic</td>
+
       <td>Dominic Schwarz</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td>Protocol:</td>
 
       <td>Protocol:</td>
       <td>restriction digest, PCR purification, ligation, chem trafo, PCR, Agarose gel</td>
+
       <td>
 +
<a href="https://static.igem.org/mediawiki/2018/7/7e/T--Munich--WL1_Restriction_Digest.pdf" target="_blank">Restriction digest</a>,  
 +
<a href="https://international.neb.com/products/t1030-monarch-pcr-dna-cleanup-kit-5-ug#Product%20Information" target="_blank">PCR purification</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/1/1a/T--Munich--WL1_Ligation.pdf" target="_blank">Ligation</a>,  
 +
<a href="https://static.igem.org/mediawiki/2018/a/a5/T--Munich--WL1_Chemical_transformation.pdf" target="_blank">Chemical Transformation</a>,  
 +
<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>
 +
</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td>Notes:</td>
 
       <td>Notes:</td>
       <td> digest with XbaI, SpeI <br>
+
       <td> Digest with XbaI, SpeI <br>
transformation of Dh5a
+
Transformation of Dh5a
 
</td>
 
</td>
 
     </tr>
 
     </tr>
 
  <tr>
 
  <tr>
       <td>Results:</td>
+
       <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td>
       <td>No bands on the Gel. Colonies on the plate resulted from contamination.</td>
+
       <td>No bands on the Gel. Colonies on the plate resulted from contamination (religation of backbound).</td>
 
     </tr>
 
     </tr>
 
</table>
 
</table>

Latest revision as of 23:57, 17 October 2018

Forming Oligodimers from Single-Strand DNA chi6 Sequences

2018/06/01
Participants: Dominic Schwarz
Protocol: Oligodimerization
Notes: Oligodimers were bought

Assembling pSB1C3_Chi6 with A3 Assembly

2018/06/04
Participants: Dominic Schwarz
Protocol: Restriction digest, Ligation, Chemical transformation, Miniprep, Sequencing
Notes: pSB1C3 Backbone was generated by restriction with XbaI and SpeI. Chi6 Dimers were digested with XbaI & SpeI.
Transformation of Dh5a
Results: No sequence obtained for the given primers. The samples must be contaminated. We decided to redo the experiment.

Redo: Assembling pSB1C3_Chi6 with A3 Assembly

2018/06/06 - 2018/06/26
Participants: Dominic Schwarz
Protocol: Restriction digest, PCR purification, Ligation, Chemical Transformation, PCR, Agarose gel
Notes: Digest with XbaI, SpeI
Transformation of Dh5a
Results: No bands on the Gel. Colonies on the plate resulted from contamination (religation of backbound).