Team:Cambridge

From 2009.igem.org

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    <h1>Overview</h1>
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    <b>Previous iGEM teams have focused on genetically engineering bacteria to respond to novel inputs – for example light, or biologically significant compounds. There is an unmistakable need, therefore, to also develop clear, user-friendly outputs, especially for use with biosensors.  The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy.  However, how much easier would it be if we could simply ''see'' the output with our own eyes?  The Cambridge 2009 iGEM team is engineering E. coli to produce a range of pigments in order to equip future projects with better, more reliable, discrete outputs under logic control.  Further, our bacteria utilize a shutter mechanism that guarantees pigment production after just a brief exposure to the desired input.  </b>
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          <h1>Project A</h1>
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Under construction <br /><b> Under construction </b> <a href="https://2009.igem.org/Team:Cambridge/ProjectA"> Read on...</a>
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          <h1>Project B</h1>
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Under construction. <br /><b> Under construction. </b> <a href="https://2009.igem.org/Team:Cambridge/ProjectB"> Read on...</a>
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          <h1>Project C</h1>
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Under construction<br /> <b> Under construction. </b>
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<a href="https://2009.igem.org/Team:Cambridge/ProjectC"> Read on...</a>
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          <h1>Modelling</h1>
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Under construction.</b> <a href="https://2009.igem.org/Team:Cambridge/Modelling">Read on...</a>
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    <td width="200"><a href="http://www.labtech.co.uk/" class="noborder"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/labtech.jpg" alt="labtech" width="131" height="17"></a></td>
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    <td width="200"><a href="http://www.clontech-europe.com/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/clontech.jpg" alt="Clontech" width="112" height="34"></a></td>
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  <td width ="200"><a href="http://www.expressys.com/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/expressys.jpg" alt="expressys" width="112" height="70"></a></td>
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    <td><a href="http://www.invitrogen.com/site/us/en/home.html"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/invirtogen.jpg" alt="invitrogen" width="160" height="25"></a></td>
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    <td><a href="http://www.medical-solutions.co.uk/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/geneservice.jpg" alt="geneservice" width="140" height="26"></a></td>
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    <td><a href="http://www.bioscience.co.uk/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/cambridgebioscience.jpg" alt="cambridge bioscience" width="157" height="42"></a></td>
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    <td><a href="http://www.zymoresearch.com/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/zymoresearch.jpg" alt="zymo research" width="135" height="45"></a></td>
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    <td><a href="http://www.vwr.com/index.htm"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/vwr.jpg" alt="VWR" width="140" height="47"></a></td>
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    <td><a href="http://www.microzone.co.uk/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/microzone.gif" alt="Microzone" width="131" height="44"></a></td>
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    <td><a href="http://www.finnzymes.com/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/finnzymes.jpg" alt="Finnzymes" width="131" height="43"></a></td>
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    <td><a href="http://www.fisher.co.uk/"><img src="http://www.gen.cam.ac.uk/Images/logos/iGEMsponsors/fisherscientific.jpg" alt="Fisher Scientific" width="132" height="33" /></a></td>
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    <td><a href="http://www.dna20.com/"><img src="http://openwetware.org/images/8/88/Dna20_logo.jpg" alt="DNA 2.0" width="132" height="66" /></a></td>
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Revision as of 10:48, 21 July 2009

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Cam09logo.png

Previous iGEM teams have focused on genetically engineering bacteria to respond to novel inputs – for example light, or biologically significant compounds. There is an unmistakable need, therefore, to also develop clear, user-friendly outputs, especially for use with biosensors. The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy. However, how much easier would it be if we could simply see the output with our own eyes? The Cambridge 2009 iGEM team is engineering E. coli to produce a range of pigments in order to equip future projects with better, more reliable, discrete outputs under logic control. Further, our bacteria utilize a shutter mechanism that guarantees pigment production after just a brief exposure to the desired input.

Your team picture
Team Example


Home The Team The Project Parts Submitted to the Registry Modelling Notebook Protocols

(Or you can choose different headings. But you must have a team page, a project page, and a notebook page.)

Template:Cambridge/Notitle

Template:Cambridge09

Overview

Previous iGEM teams have focused on genetically engineering bacteria to respond to novel inputs – for example light, or biologically significant compounds. There is an unmistakable need, therefore, to also develop clear, user-friendly outputs, especially for use with biosensors. The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy. However, how much easier would it be if we could simply ''see'' the output with our own eyes? The Cambridge 2009 iGEM team is engineering E. coli to produce a range of pigments in order to equip future projects with better, more reliable, discrete outputs under logic control. Further, our bacteria utilize a shutter mechanism that guarantees pigment production after just a brief exposure to the desired input.

Project A

Under construction
Under construction Read on...

Project B

Under construction.
Under construction. Read on...

Project C

Under construction
Under construction. Read on...

Modelling

Under construction. Read on...
labtech Clontech expressys
invitrogen geneservice cambridge bioscience
zymo research VWR Microzone
Finnzymes Fisher Scientific DNA 2.0

Retrieved from "http://2009.igem.org/Team:Cambridge"