Difference between revisions of "Team:HK SSC/Design"

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<h1 style="color: purple; font-size: 25px;">Design</h1>
 
<h1 style="color: purple; font-size: 25px;">Design</h1>
 
<h1><u>Expression of dCas9-sgRNA-GFP Complex for gene silencing</u></h1>
 
<h1><u>Expression of dCas9-sgRNA-GFP Complex for gene silencing</u></h1>
<p>We designed a plasmid that can be expressed in both E.coli cells and Microcystis Aeruginosa cells, encoding dCas9, green fluorescence protein and an sgRNA targeting McyB.
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<p>We designed a plasmid that can be expressed in both E.coli cells and Microcystis Aeruginosa cells, encoding dCas9, green fluorescence protein and an sgRNA targeting McyB.</p>
 
</br>
 
</br>
Our plasmid is cloned by assembling 3 parts: the shuttle vector, the dCas9-GFP complex and the sgRNA. </p>
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<p>Our plasmid is cloned by assembling 3 parts: the shuttle vector, the dCas9-GFP complex and the sgRNA. </p>
  
 
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Revision as of 08:34, 21 October 2019

Design

Expression of dCas9-sgRNA-GFP Complex for gene silencing

We designed a plasmid that can be expressed in both E.coli cells and Microcystis Aeruginosa cells, encoding dCas9, green fluorescence protein and an sgRNA targeting McyB.


Our plasmid is cloned by assembling 3 parts: the shuttle vector, the dCas9-GFP complex and the sgRNA.