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Team:BostonU/Results
From 2013.igem.org
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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 and __ number of Level 2 Devices | + | <br>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> __ number of Level 1 Transcriptional Units and __ number of Level 2 Devices |
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<br>From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in <i>E. coli</i> | <br>From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in <i>E. coli</i> | ||
Revision as of 19:59, 4 September 2013
Results Summary
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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 MoClo Library We have also updated the MoClo Kit 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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Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully characterized __ number of Level 1 Transcriptional Units and __ number of Level 2 Devices From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in E. coli |
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Working closely with the Purdue Biomakers team, we have designed a data sheet 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 |
