Difference between revisions of "Team:UCC Ireland/Collaborations"

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<h1 style='text-align: center;'>École Polytechnique Fédérale de Lausanne</h2>
  
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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2017.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2017.igem.org/Judging/Awards"> award listed above</a>. </p>
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<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2017.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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We collaborated with École Polytechnique Fédérale de Lausanne in Switzerland whose project focuses heavily on using cell-free systems. During the course of our collaboration, we discussed how cell-free systems could be beneficial to both our projects, enabling our systems to be used more widely and with more ease than if they were implemented in live bacterial chassis’. We also discussed cell-free protocols and reporter systems that could be used.  
 
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<h1>Collaborations</h1>
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Sharing and collaboration are core values of iGEM. We encourage you to reach out and work with other teams on difficult problems that you can more easily solve together.
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<h3>Silver Medal Criterion #2</h3>
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Specifically, the EPFL iGEM team asked us to review their cell-free protocol and compare it to what we would use with our cell-free collaborator Dr. Thomas Meaney, who aims to bring cell-free technology to a wider market. This comparison of cell-free protocols will help them to optimise their cell-free extraction and build out their project.
Complete this page if you intend to compete for the silver medal criterion #2 on collaboration. Please see the <a href="https://2017.igem.org/Judging/Medals">2017 Medals Page</a> for more information.  
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Through the course of our discussions, we learned that the EPFL team had tried to use chromoproteins in their cell free system with limited success. This has informed the future design of our biosensor strategy and has made us aware that we need to be careful in using amilCP as a reporter system and has made us aware that optimisation of the cell-free chassis may be required.
<h4> Which other teams can we work with? </h4>
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You can work with any other team in the competition, including software, hardware, high school and other tracks. You can also work with non-iGEM research groups, but they do not count towards the iGEM team collaboration silver medal criterion.
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In order to meet the silver medal criteria on helping another team, you must complete this page and detail the nature of your collaboration with another iGEM team.
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Overall, our discussions and sharing of ideas were mutually beneficial in the future design and implementation of both our projects and we are very thankful to EPFL for their time.
 
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Here are some suggestions for projects you could work on with other teams:
 
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<li> Improve the function of another team's BioBrick Part or Device</li>
 
<li> Characterize another team's part </li>
 
<li> Debug a construct </li>
 
<li> Model or simulating another team's system </li>
 
<li> Test another team's software</li>
 
<li> Help build and test another team's hardware project</li>
 
<li> Mentor a high-school team</li>
 
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Latest revision as of 00:52, 2 November 2017

UCC iGEM 2017

École Polytechnique Fédérale de Lausanne

We collaborated with École Polytechnique Fédérale de Lausanne in Switzerland whose project focuses heavily on using cell-free systems. During the course of our collaboration, we discussed how cell-free systems could be beneficial to both our projects, enabling our systems to be used more widely and with more ease than if they were implemented in live bacterial chassis’. We also discussed cell-free protocols and reporter systems that could be used.

Specifically, the EPFL iGEM team asked us to review their cell-free protocol and compare it to what we would use with our cell-free collaborator Dr. Thomas Meaney, who aims to bring cell-free technology to a wider market. This comparison of cell-free protocols will help them to optimise their cell-free extraction and build out their project.

Through the course of our discussions, we learned that the EPFL team had tried to use chromoproteins in their cell free system with limited success. This has informed the future design of our biosensor strategy and has made us aware that we need to be careful in using amilCP as a reporter system and has made us aware that optimisation of the cell-free chassis may be required.

Overall, our discussions and sharing of ideas were mutually beneficial in the future design and implementation of both our projects and we are very thankful to EPFL for their time.