Team:UNITN-Trento

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<li><a href="https://2012.igem.org/Team:UNITN-Trento/DataPage">Data Page</a></li>
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<li class="folder"><a href="javascript:void(0);">Parts</a>
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<li><a href="https://igem.org/Team.cgi?id=731">Team Profile</a></li>
<li><a href="https://igem.org/Team.cgi?id=731">Team Profile</a></li>
<li><a href="https://2012.igem.org/Team:UNITN-Trento/Trento">Where We Are</a></li>
<li><a href="https://2012.igem.org/Team:UNITN-Trento/Trento">Where We Are</a></li>
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<li><a href="https://2012.igem.org/Team:UNITN-Trento/Press">Press</a></li>
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<li><a href="https://2012.igem.org/Team:UNITN-Trento/Safety">Safety</a></li>
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<li><a href="https://2012.igem.org/Team:UNITN-Trento/Safety">Safety</a></li>
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<li><a href="https://2012.igem.org/Team:UNITN-Trento/H2S">H<sub>2</sub>S</a></li>
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<li><a href="https://2012.igem.org/Team:UNITN-Trento/Outreach">Outreach</a></li>
<li><a href="https://2012.igem.org/Team:UNITN-Trento/Outreach">Outreach</a></li>
<li><a href="https://2012.igem.org/Team:UNITN-Trento/Art">Art&Science</a></li>
<li><a href="https://2012.igem.org/Team:UNITN-Trento/Art">Art&Science</a></li>
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<p>Design by Jason Fontana. Powered by <a href="http://www.mediawiki.org/wiki/MediaWiki">MediaWiki</a>. This website is under the <a href="http://creativecommons.org/licenses/by/3.0/">CC Attribution licence</a>.<!-- | <span class="toggle">Toggle controls</span>--></p>
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Revision as of 18:02, 20 September 2012

iGEM Trento

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Saving the World, one statue at a time


Project Codename: Crust Away

Statues and monuments all over the world are not enjoyed to the extent that they should be because they are covered in a disfiguring black crust, which consists mainly of CaSO4.
A practical solution would be if a cheap mechanism was available to continually remove the pollutant molecules that adhere to the surface of statues. To build such a system, we are engineering an aerobic sulfur reducing pathway in E. coli to dissolve the disfiguring black crusts.

Read More

Project Codename: Terminator 5

Surprisingly little standardization of T7 phage derived parts has occurred, despite the prevalence of T7 parts in recombinant technologies. Also, the compatibility between T7 and E. coli derived parts has not been explored. To better understand the compatibility of the two systems and to begin to better characterize T7 biological parts, we are measuring the termination efficiencies of T7 and E. coli transcriptional terminators with E. coli and T7 RNA polymerases.

Read More

MEET THE TEAM

ACHIEVEMENTS


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