McGill University 2006

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EDITED BY ASHWIN. If you want to change it, feel free :)-->
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<center><h2>Projects</h2></center>
<center><h2>Projects</h2></center>
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* '''Team 1: Split YFP'''
* '''Team 1: Split YFP'''
The idea behind the project is fluorescence complementation, which involves the joining of two leucine zipper proteins Jun and Fos each fused to a half terminus of YFP.  
The idea behind the project is fluorescence complementation, which involves the joining of two leucine zipper proteins Jun and Fos each fused to a half terminus of YFP.  
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Jun-beta and the Fos-beta respectively.
Jun-beta and the Fos-beta respectively.
We transformed two cell populations, one expressing Jun-beta-YFPN and the other expressing Fos-beta-YFPC.These two cell populations were combined and the two vectors were then expressed, ideally resulting in the fusion of the Jun and Fos leucine zipper proteins on the cell membrane when the cells are in close contact. This would result in the binding of the two halves of the YFP protein resulting in flourescence.
We transformed two cell populations, one expressing Jun-beta-YFPN and the other expressing Fos-beta-YFPC.These two cell populations were combined and the two vectors were then expressed, ideally resulting in the fusion of the Jun and Fos leucine zipper proteins on the cell membrane when the cells are in close contact. This would result in the binding of the two halves of the YFP protein resulting in flourescence.
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'''* Team 2: Repressilator'''
'''* Team 2: Repressilator'''
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[[Theory Behind the Oscillator|Theory Behind the Oscillator]]
[[Theory Behind the Oscillator|Theory Behind the Oscillator]]
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<center><h2>Lab Procedures</h2></center>
<center><h2>Lab Procedures</h2></center>

Revision as of 22:55, 27 October 2006

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Welcome to the McGill Wiki! Basically, we're a team of 12 undergrads, 1 grad student, and 1 professor who like to have fun and clone things in our spare time. McGill University is located in Montreal, Quebec, which has given us wonderful opportunities to balance lab work with festivals and general craziness. iGEM has been a great opportunity to get lab experience while having the freedom to be creative, and we look forward to meeting the other teams at the jamboree!

Clip image002.jpgDancing e copyzz.jpg



Projects

  • Team 1: Split YFP

The idea behind the project is fluorescence complementation, which involves the joining of two leucine zipper proteins Jun and Fos each fused to a half terminus of YFP. Subsequently, both of these chimeric proteins were fused to a beta gene that codes for a membrane protein. The project involved performing a PCR reaction to produce two inserts, the N-terminus and the C-terminus of the YFP, and then ligating these inserts into 2 vectors, containing the Jun-beta and the Fos-beta respectively. We transformed two cell populations, one expressing Jun-beta-YFPN and the other expressing Fos-beta-YFPC.These two cell populations were combined and the two vectors were then expressed, ideally resulting in the fusion of the Jun and Fos leucine zipper proteins on the cell membrane when the cells are in close contact. This would result in the binding of the two halves of the YFP protein resulting in flourescence.

* Team 2: Repressilator

We are working on making a biological oscillator. This system will consist of the Elowiitz repressilator and quorum sensing.

Oscillator Example

Theory Behind the Oscillator

Lab Procedures


Club


Just for Fun

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