IGEM:UC Berkeley/2006: Difference between revisions
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[[IGEM:UC Berkeley/2006/Short DNA frag cleanup|Short DNA frag cleanup]]<br> | [[IGEM:UC Berkeley/2006/Short DNA frag cleanup|Short DNA frag cleanup]]<br> | ||
[[IGEM:UC Berkeley/2006/DNA purifications|DNA purifications]]<br> | [[IGEM:UC Berkeley/2006/DNA purifications|DNA purifications]]<br> | ||
[[IGEM:UC Berkeley/2006/PCR machine program (for expansion kit)|PCR machine program (for expansion kit)]]<br> | |||
'''Subgroup Notebooks''' | '''Subgroup Notebooks''' | ||
Revision as of 13:21, 14 July 2006
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UC Berkeley We plan to create an addressable cell-to-cell communication mechanism in e.coli. Communication will be achieved through the selective swapping of two plasmids, one from each cell. When conjugation occurs a promoter will be turned on in the receiptient cell and it will express GFP thereby illuminating it and signaling that communication was successful...someone who understands this well should really write something better here. |
<html> <img src="http://openwetware.org/images/b/b9/Icon_board.png" alt="Resources"> </html>TeamUndergrads Bryan Hernandez Postdocs |
<html> <img src="http://openwetware.org/images/e/e2/Icon_info.png" alt="News" border="0"> </html>ToolsThe Details Oligonucleotides Procedures Procedure Overview (Plasmid DNA to Sequencing) Subgroup Notebooks |
<html> <img src="http://openwetware.org/images/b/b9/Icon_board.png" alt="Resources"> </html>ProjectAddressable Cell-to-Cell Communication Useful Links |
