Team:UST-Beijing/Team

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Revision as of 06:02, 5 August 2011 by Chingsong (Talk | contribs)


This is a template page. READ THESE INSTRUCTIONS.
You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples HERE.
You MUST have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.


You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.
UST-Beijing logo.png

Tell us more about your project. Give us background. Use this is the abstract of your project. Be descriptive but concise (1-2 paragraphs)

Your team picture
Team Example


Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions


Who we are



Advisors:

  • Advisor 1: ChingSong*Advisor 2: Our favorite ChingSong
  • Grad Student 1: Our leader Hanzhong Ke


Undergrads:

  • Student 1: Danyang Wang
  • Student 2: Lujun Zhou
  • Student 3: Fang Li, Is going to save the world
  • Student 4: Wenjing Zhang Loves iGEM
  • Student 5: A normal student... or(r) am I?
  • Student 6: Table football fan
  • Student 7:


UST-Beijing Team member 1.png

Team member 1

UST-Beijing Team member 2.png

Team member 2

UST-Beijing Team member 3.png

Team member 3

UST-Beijing Team member 4.png

Team member 4

UST-Beijing Team member 5.png

Team member 5

UST-Beijing Team member 6.png

Team member 6

UST-Beijing Team member 7.png

Team member 7

What we did

We using lacI DNA-binding domain and LXRbeta ligand-binding domain, we made an artificial bile acid receptor which can regulate expression of target gene within a natural lacI operon. As proof of principle, we demonstrate that regulation of bacteria gene expression by host eukaryocyte metabolites is achievable using chimeric nuclear receptors. Through directed molecular evolution, a harmonious signal network regulating metabolism of both prokaryocytes and their host eukaryocytes in the digestive tract is feasible.

Where we're from

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