McGill
From 2007.igem.org
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== Project Overviews == | == Project Overviews == | ||
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<u>'''Team 1 - Fluorescence Complimentation'''</U> | <u>'''Team 1 - Fluorescence Complimentation'''</U> | ||
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[[McGill/Team_1_Background_Papers|Background Papers]] <br> | [[McGill/Team_1_Background_Papers|Background Papers]] <br> | ||
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<u>'''Team 2 - Repressilator'''</u> | <u>'''Team 2 - Repressilator'''</u> | ||
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<center>Please feel free to check out our work from last year at [https://2006.igem.org/wiki/index.php/McGill_University iGEM McGill 2006]</center><br> | <center>Please feel free to check out our work from last year at [https://2006.igem.org/wiki/index.php/McGill_University iGEM McGill 2006]</center><br> | ||
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== In the Lab == | == In the Lab == | ||
[[McGill/Lab Notebook|Lab Notebook]]<br> | [[McGill/Lab Notebook|Lab Notebook]]<br> | ||
[[McGill/Lab Protocols|Lab Protocols]] | [[McGill/Lab Protocols|Lab Protocols]] | ||
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== The Team == | == The Team == | ||
[[McGill/Team Roster| Team Roster]]<br> | [[McGill/Team Roster| Team Roster]]<br> | ||
[[McGill/Mailing List|Mailing List]] | [[McGill/Mailing List|Mailing List]] | ||
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Revision as of 23:02, 19 May 2007
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 reversibly 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. More Information
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