Difference between revisions of "Team:CSU Fort Collins/InterLab"

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<h2>Experimental Approach</h2>
  
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<p>The Interlab Study protocols that were followed can be found in the notebook. The plate reader
<h3>★  ALERT! </h3>
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portion that was followed can be found here (please put protocol link here).
<p>This page is used by the judges to evaluate your team for the <a href="https://2017.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2017.igem.org/Judging/Awards"> award listed above</a>. </p>
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Results</p>
<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2017.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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<p>All of the test devices, including the negative and positive control plates with growing colonies
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were given to us by the University of Colorado Boulder team. We were unable to successfully
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transform competent E. coli cells with all of the plasmids. After following the protocols to grow
 
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the cultures, samples were taken from each test device at hour 0, 2, 4, and 6. Unfortunately,
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the fluorescence of the colonies were not measured correctly so we were not able to
<h1>InterLab</h1>
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contribute to the interlab study data.
<h3>Bronze Medal Criterion #4</h3>
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<p><b>Standard Tracks:</b> Participate in the Interlab Measurement Study and/or improve the characterization of an existing BioBrick Part or Device and enter this information on that part's Main Page in the Registry. The part that you are characterizing must NOT be from a 2017 part number range.
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For teams participating in the <a href="https://2017.igem.org/Competition/InterLab_Study">InterLab study</a>, all work must be shown on this page.  
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Revision as of 04:10, 1 November 2017

Experimental Approach

The Interlab Study protocols that were followed can be found in the notebook. The plate reader portion that was followed can be found here (please put protocol link here). Results

All of the test devices, including the negative and positive control plates with growing colonies were given to us by the University of Colorado Boulder team. We were unable to successfully transform competent E. coli cells with all of the plasmids. After following the protocols to grow the cultures, samples were taken from each test device at hour 0, 2, 4, and 6. Unfortunately, the fluorescence of the colonies were not measured correctly so we were not able to contribute to the interlab study data.