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Team:MIT phage context
From 2010.igem.org
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<b>WORK FROM OTHER IGEM TEAMS</b> | <b>WORK FROM OTHER IGEM TEAMS</b> | ||
<br> | <br> | ||
| - | + | The following teams have used some component of our phage system previously. No other teams have used our method of polyphage with incorporated leucine zippers for polymerization. | |
<br><br> | <br><br> | ||
| - | + | <ul> | |
| + | <li> | ||
| + | In 2006 the McGill team attempted to use leucine zippers fused to split YFP to display on cells and cause the cells to adhere via the split YFP. See: http://parts.mit.edu/wiki/index.php/McGill_University_2006</li> | ||
<br><br> | <br><br> | ||
| - | Paris's team in 2009 attempted to use Jun/Fos as a snare; Jun on signal vesicle, Fos on membrane of receiving cell. See: https://2009.igem.org/Team:Paris#top | + | <li> |
| + | The 2009 Freiburg Bioware team used Fos/Jun for a 'programmable enzyme' using Fok-fused Fos/Jun as factor in DNA cleavage. See: https://2009.igem.org/Team:Freiburg_bioware/Project/FOS</li> | ||
| + | <br><br> | ||
| + | <li> | ||
| + | Paris's team in 2009 attempted to use Jun/Fos as a snare; Jun on signal vesicle, Fos on membrane of receiving cell. See: https://2009.igem.org/Team:Paris#top</li> | ||
| + | </ul> | ||
</td> | </td> | ||
</table> | </table> | ||
Revision as of 19:52, 24 October 2010
iGEM 2010
hairy cells and polymerizing phage - Context |
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WORK FROM OTHER IGEM TEAMS The following teams have used some component of our phage system previously. No other teams have used our method of polyphage with incorporated leucine zippers for polymerization.
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