Difference between revisions of "Team:EPF Lausanne/Notebook/Yeast"

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                     <ul class="nav nav-pills nav-stacked" data-spy="affix" data-offset-top="200" data-offset-bottom="600">
 
                     <ul class="nav nav-pills nav-stacked" data-spy="affix" data-offset-top="200" data-offset-bottom="600">
 
                         <li class="active"><a href="#integrate_pTPGI_dCas9_VP64">Integrate pTPGI_dCas9_VP64</a></li>
 
                         <li class="active"><a href="#integrate_pTPGI_dCas9_VP64">Integrate pTPGI_dCas9_VP64</a></li>
                         <ul>
+
                         </ul>
 
                         <li <a href="#Integrate_reporter_plasmid">Integrate reporter plasmid</a></li>
 
                         <li <a href="#Integrate_reporter_plasmid">Integrate reporter plasmid</a></li>
 
                         </u1>
 
                         </u1>
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                             <li><a href="#gibsonprom">Gibson assembly of promoters in reporter plasmid</a></li>
 
                             <li><a href="#gibsonprom">Gibson assembly of promoters in reporter plasmid</a></li>
 
                             <li><a href="#integrate_reporters_plasmids">Integrate the reporter plasmids</a></li>
 
                             <li><a href="#integrate_reporters_plasmids">Integrate the reporter plasmids</a></li>
                         <ul>
+
                         </ul>
 
                         <li><a href="#Integrate_and_express_gRNAs">Integrate and express gRNAs</a></li>
 
                         <li><a href="#Integrate_and_express_gRNAs">Integrate and express gRNAs</a></li>
 
                         </ul>
 
                         </ul>

Revision as of 14:21, 17 August 2015

EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits

saccharomyces cerevisiae

pTPGI_dCas9_VP64 integration

As we need dCas9 expressing yeasts, we decided to integrate a plasmid that would inducively express dCas9.

First and second trial

The negative and positive control worked fine, but the transformation control didn’t work. After investigation we found out that we didn’t have an origin of replication in our plasmid thus not enabling our yeasts to replicate the plasmid and to grow. See more details here

EPFL 2015 iGEM bioLogic Logic Orthogonal gRNA Implemented Circuits