McGill
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== Project Overviews == | == Project Overviews == | ||
- | '''Team 1 - | + | '''Team 1 - Fluorescence Complimentation''' |
- | + | This project on fluorescence complementation involves confirming previous work using Jun and Fos heterodimerizing proteins, each fused to a half terminus of YFP. The two halves of the YFP protein bind, giving rise to fluorescence. We will then carry out the experiment with GFP or YFP split at different points in order to find a cleavage point that produces reversible fluorescence. These half proteins will then be attached to proteins that revesibly associate.<br> | |
- | |||
- | '''Team 2 - | + | '''Team 2 - Repressilator''' |
- | + | Our project consists of a two-gene oscillator with coupling by an autoinducer (AI). This system was presented last year. We will test the effects of adding AI and Tetracycline to the medium. We will also investigate the nature of the oscillations at different cell densities.<br> | |
+ | |||
+ | [[McGill/Background|Background]] |
Revision as of 04:10, 16 May 2007
Contents |
Message Board (temporary)
Guys, when you make the links for the wiki pages, please follow this example:
[[McGill/Link_to_page|Display Name]]
An actual link would look like this in wiki code: [[McGill/Team_1:_Fluorescence_Complementation|Team 1: Fluorescence Complementation]]
Thanks! - Hanmo
I'll chop up Adam's PDF on my break today to put it into the Protocols section. Tim
Hello Tim,
we need a lab notebook page, protocols page and team members page, etc.
PS: Everyone, get a lab notebook! We're making our cells chemically competent tomorrow so if you want to see/help out then show up around 10:30. Horiavulpe 16:41, 14 May 2007 (EDT)
Note from iGEM: Please use the format "McGill/Page Name" for all the pages your team uses. I fixed
teh Lab Protocols, the Lab Notebook, and the Team Roster links. Thanks, - Randy
In the Lab
The Team
Project Overviews
Team 1 - Fluorescence Complimentation
This project on fluorescence complementation involves confirming previous work using Jun and Fos heterodimerizing proteins, each fused to a half terminus of YFP. The two halves of the YFP protein bind, giving rise to fluorescence. We will then carry out the experiment with GFP or YFP split at different points in order to find a cleavage point that produces reversible fluorescence. These half proteins will then be attached to proteins that revesibly associate.
Team 2 - Repressilator
Our project consists of a two-gene oscillator with coupling by an autoinducer (AI). This system was presented last year. We will test the effects of adding AI and Tetracycline to the medium. We will also investigate the nature of the oscillations at different cell densities.