Team:BostonU/Results

From 2013.igem.org

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<h2>Results Summary</h2>
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<h7><p>Below is a brief summary of our results from this summer. Each statement has a link shown in </h7><h8>RED</h8><h7> to the page(s) containing more information and detailed results. </h7> </p>
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<h5>MoClo Library and Kit</h5>
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<br>This summer, we have created and submitted __ number of new Level 0 Parts, __ number of new Destination Vectors, __ number of new Level 1 Transcriptional Units, and __ number of Level 2 Devices to the <a href="https://2013.igem.org/Team:BostonU/Parts">MoClo Library</a>
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<br><p>This summer, we created 63 new Level 0 Parts (32 prom, 12 5'UTR, 16 CDS, and 3 terminators), 14 new Destination Vectors, and 86 new Level 1 Transcriptional Units to the <a href="https://2013.igem.org/Team:BostonU/Parts">MoClo Library</a></p>
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<p>We have also updated the <a href="https://2013.igem.org/Team:BostonU/MoClo">MoClo Kit</a> to include 90 Level 0 Basic Parts and 21 Destination Vectors so teams next year can create devices containing up to 4 transcriptional units</p>
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<br>We have also updated the <a href="https://2013.igem.org/Team:BostonU/MoClo">MoClo Kit</a> to include __ number of Level 0 Basic Parts and __ number of Destination Vectors so teams next year can create devices containing up to 5 transcriptional units
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<h5>Characterization Data</h5>
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<br>Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we characterized __ number of Level 1 Transcriptional Units
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<br><p>Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully <a href="https://2013.igem.org/Team:BostonU/Data">characterized</a> 64 Level 1 Transcriptional Units and 2 Level 2 Devices</p>
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<p>From this work, we will draft a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in <i>E. coli</i></p>
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<h5>Data Sheet Creation</h5>
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<br>Working closely with the <a href="https://2013.igem.org/Team:Purdue">Purdue Biomakers</a> team, we have designed a data sheet for the iGEM community and beyond
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<br><p>Working closely with the <a href="https://2013.igem.org/Team:Purdue">Purdue Biomakers</a> team, we are designing a <a href="https://2013.igem.org/Team:BostonU/DataSheet">datasheet</a> that will allow users to more easily share information and data within the iGEM community and beyond</p>
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<p>We have begun implementing a Java-based web tool to generate these data sheets</p>
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Latest revision as of 03:29, 28 September 2013



Results Summary

Below is a brief summary of our results from this summer. Each statement has a link shown in RED to the page(s) containing more information and detailed results.




      This summer, we created 63 new Level 0 Parts (32 prom, 12 5'UTR, 16 CDS, and 3 terminators), 14 new Destination Vectors, and 86 new Level 1 Transcriptional Units to the MoClo Library

      We have also updated the MoClo Kit to include 90 Level 0 Basic Parts and 21 Destination Vectors so teams next year can create devices containing up to 4 transcriptional units



      Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully characterized 64 Level 1 Transcriptional Units and 2 Level 2 Devices

      From this work, we will draft a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in E. coli



      Working closely with the Purdue Biomakers team, we are designing a datasheet that will allow users to more easily share information and data within the iGEM community and beyond

      We have begun implementing a Java-based web tool to generate these data sheets