Team:UANL Mty-Mexico BETA

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<a href="https://2014.igem.org/Team:UANL_Mty-Mexico/Project" style="text-decoration:none;color:#1C140D">PROJECT</a> </td>
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<h3>Welcome!  <br>Team:UANL Mty-Mexico</h3>
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<h3>Read about our projects!</h3>
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One E.coli Has One Function
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What is our project at 2014?
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Cadmium is one of harmful materials for us. 50 years ago, itai-iati disease was going around in center of Japan Gihu. The cause was industrial wastewater. Cadmium contained the water. Our project is to find a way to clean contaminated with Cadmium. we think how to clean the water. We use E.coli.
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Concretely, we use two kinds of E.coli. One catches Cadmium. the Other makes to all E.coli to use chemoattractant. Catches E.coli displays metallothionein (metallothionein is a protein that combines a heavy metal. Cadomium is one kind of heavy metal). Other is releasing Asp (Asp is one kind of chemoattractant. All E.coli is close to the Asp E.coli).
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To use these E.coli. Finally cadomiun is catched(wastewater is be clean).
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What experiment we did?
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・How to check E.coli's chemotaxis?
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We make use of other igem team’s assay.
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Using soft agar plate.we let E.coli siwm.
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・We made a plasmid
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Our project need to two kind of plasmid.
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we made one plasmid.And we have to make one more plasmid.
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<li id="Link0" class="SlideLink">Background</li><li id="Link1" class="SlideLink">Problem</li><li id="Link2" class="SlideLink">Idea</li><li id="Link3" class="SlideLink">Solution</li>
 
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<h2><b>OVERVIEW</b></h2>
 
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In order to be capable of controlling transformed bacteria and reprogram its function as many times as would be required, we designed a system consisting of a bacteriophage that infects just one specific strain of bacteria and has on its genome the information to codify a TALEN/ZFN enzyme and a reporter gene. With this tools (TALEN/ZFN) we can target a specific sequence of the host's plasmids to degrade them. The bacteriophages will replace the plasmids, giving it a new function or characteristic that could be a totally new one.
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<a href="https://2013.igem.org/Team:Calgary/Project/OurSensor">
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<h2>Our Sensor</h2>
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<a href="#firstblock" style="text-decoration:none;color:#1C140D"> Top </a> </td></tr>
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<p>Check out what we did in the lab this summer to detect <i>E. coli</i> contamination! Learn about the design of our detector, linker, and reporter as well as our prototype and modelling.</p>
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<h2>Final System</h2>
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<p>We have shown our final system in action! Click here to see our modeling, talks with industry, and characterization data combine to make a biosensor that can detect DNA in under 5 minutes!</p>
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<p>Check out how Human Practices helped guide the development of our project. Learn how we spent time talking to various experts in the industry to design our project with our end-user in mind.</p>
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<p>We worked hard with the Paris-Bettencourt team this season to develop useful tools for the rest of the iGEM community. Click here to find out what our collaboration can add to iGEM. </p>
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<h2 style="text-align: center;">Thank You to Our Sponsors</h2>
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Latest revision as of 19:40, 16 October 2014

Welcome!
Team:UANL Mty-Mexico

Read about our projects!

One E.coli Has One Function What is our project at 2014? Cadmium is one of harmful materials for us. 50 years ago, itai-iati disease was going around in center of Japan Gihu. The cause was industrial wastewater. Cadmium contained the water. Our project is to find a way to clean contaminated with Cadmium. we think how to clean the water. We use E.coli. Concretely, we use two kinds of E.coli. One catches Cadmium. the Other makes to all E.coli to use chemoattractant. Catches E.coli displays metallothionein (metallothionein is a protein that combines a heavy metal. Cadomium is one kind of heavy metal). Other is releasing Asp (Asp is one kind of chemoattractant. All E.coli is close to the Asp E.coli). To use these E.coli. Finally cadomiun is catched(wastewater is be clean). What experiment we did? ・How to check E.coli's chemotaxis? We make use of other igem team’s assay. Using soft agar plate.we let E.coli siwm. ・We made a plasmid Our project need to two kind of plasmid. we made one plasmid.And we have to make one more plasmid.
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