Difference between revisions of "Team:UNOTT/Results"

 
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{{:Team:UNOTT/Template/NavBarTest}}
 
{{:Team:UNOTT/Template/NavBarTest}}
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<center>
 
<p><span style="color: #ffffff;">&nbsp;</span></p>
 
<h1 style=>Results coming soon..</h1>
 
  
<img src="https://static.igem.org/mediawiki/2017/0/0d/T--UNOTT--GIF.gif">
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</center>
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</p>
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<div class="image">
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<div class="crop">
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    <img src="https://static.igem.org/mediawiki/2017/0/03/T--UNOTT--Results.jpeg"; style:""width:100%;height:auto;">
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</div>
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<h2><span>RESULTS:<span class='spacer'></span></h2>
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<div class="wrapper">
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  <div class="dropdown1">
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  <input type="checkbox" id="question-1">
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  <label for="question-1"> STEP 1: Create guideRNA Plasmid </label>
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    <div class="text">
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      <p>Text</p>
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<br> 
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  <input type="checkbox" id="question-2">
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  <label for="question-2"> STEP 2: Create Reporter Plasmid </label>
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      <p>Text</p>
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  <label for="question-3">  STEP 3: Create Promoter Library </label>
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      <p>Text</p>
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  <label for="question-4">STEP 4: Random Ligations      </label>
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      <p>Text</p>
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  <label for="question-5">STEP 5: Freeze drying & Revival    </label>
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      <p>Here are the results of our freeze-dried cells revival experiments. With these experiments, we want to show that different storage do not have an effect on the revival of the cells within our key.</p>
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  <label for="question-6"> STEP 6: CRISPRi & guideRNA efficiency    </label>
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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,
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or with a non-targeting gRNA plasmid.</p>
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<img src="https://static.igem.org/mediawiki/2017/6/6a/T--UNOTT--gRNAresultspic.jpeg">
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<img src="https://static.igem.org/mediawiki/2017/e/e1/T--UNOTT--photosofgRNAresults.jpeg">
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{{:Team:UNOTT/Template/Footer}}
 
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Latest revision as of 16:11, 31 October 2017





RESULTS: