Team:Paris Bettencourt
From 2013.igem.org
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<a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Phage_Sensor"> | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Phage_Sensor"> | ||
- | <div id="pspanel" class="subpanel2" style="background:rgb(250,247,186) | + | <div id="pspanel" class="subpanel2" style="background:rgb(250,247,186);"> |
DETECT | DETECT | ||
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</a> | </a> | ||
<a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Drug_Screening"> | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Drug_Screening"> | ||
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TARGET | TARGET | ||
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- | Visit our Results! | + | <img width="70px" src="https://static.igem.org/mediawiki/2013/d/d5/PB_handresults.gif"/>Visit our Results! |
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</div> | </div> |
Revision as of 15:57, 22 September 2013
Tuberculosis is an infectious disease caused by Mycobacterium tuberculosis affecting millions of people over the world. Using Escherichia coli as a model organism we are developing different approaches that could contribute to the fight against TB.
A biosensor that detects the presence of sequence specific antibiotic resistance genes.
A safe and specific high-throughput drug screening method that targets essential mycobacterial metabolic proteins.
A phage system with low fitness cost producing sRNA, which inhibit the synthesis of antibiotic resistance proteins.
An E. coli which invades macrophages and kills mycobacteria.
DETECT
TARGET
SABOTAGE
INFILTRATE
Visit our Results!