Team:BostonU/Results

From 2013.igem.org

(Difference between revisions)
Line 26: Line 26:
<tr><td><img src="https://static.igem.org/mediawiki/2013/d/d8/Char_data_BU.gif" width="200px"></td>
<tr><td><img src="https://static.igem.org/mediawiki/2013/d/d8/Char_data_BU.gif" width="200px"></td>
<td><h7><ul>
<td><h7><ul>
-
<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
+
<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>
<br>
 +
<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>
</ul></td></tr></table></div></p></ul>
</ul></td></tr></table></div></p></ul>

Revision as of 19:53, 4 September 2013



Results Summary

MoClo Library and Kit


      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

Characterization Data


      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

      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

Data Sheet Creation


      Working closely with the Purdue Biomakers team, we have designed a data sheet for the iGEM community and beyond