Difference between revisions of "Team:UNOTT/Results"

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  <h4>STEP 5: Freeze drying & Revivial</h4>
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   <h4>STEP 6: CRISPRi & guideRNA efficiency</h4>
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<p>This picture shows our gRNAs working visually, but the graphs show the results of RFP detection using a microplate reader on cultures containing each of the dCas9 plasmids with one promoter-RFP-terminator brick, with its corresponding gRNA plasmid,
 
<p>This picture shows our gRNAs working visually, but the graphs show the results of RFP detection using a microplate reader on cultures containing each of the dCas9 plasmids with one promoter-RFP-terminator brick, with its corresponding gRNA plasmid,
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   <label for="question-3"> <h4> STEP 3: Create Promoter Library</h4> </label>
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   <label for="question-4"><h4>STEP 4: Random Ligations      </h4> </label>
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  <label for="question-6"> STEP 6: CRISPRi & guideRNA efficiency    </label>
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Revision as of 20:27, 29 October 2017





RESULTS:

This picture shows our gRNAs working visually, but the graphs show the results of RFP detection using a microplate reader on cultures containing each of the dCas9 plasmids with one promoter-RFP-terminator brick, with its corresponding gRNA plasmid, or with a non-targeting gRNA plasmid.