Team:Evry/Achievements
From 2012.igem.org
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- | <li>We brought a new multicellular chassis to iGEM</li> | + | <li>We brought a new multicellular <a href="https://2012.igem.org/Team:Evry/FrenchFrog">chassis</a> chassis to iGEM</li> |
- | <li>We submitted 28 biobricks to the registry, including the first working Xenopus biobricks</li> | + | <li>We submitted <a href="https://2012.igem.org/Team:Evry/Parts">28 biobricks</a> to the registry, including the first working Xenopus biobricks</li> |
<li>We characterized 12 Biobricks: | <li>We characterized 12 Biobricks: | ||
<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K812000">BBa_K812000</a>, | <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K812000">BBa_K812000</a>, |
Revision as of 01:56, 27 September 2012
iGEM Evry 2012 achievements
Asides from having lots of fun, meeting great people, gathering around cheese and wine and lazying around the Genopole gardens during lunch break, we also did a little bit of work. Here is a list of our achievements:
- We brought a new multicellular chassis chassis to iGEM
- We submitted 28 biobricks to the registry, including the first working Xenopus biobricks
- We characterized 12 Biobricks: BBa_K812000, BBa_K812050, BBa_K812010, BBa_K812030, BBa_K81203, BBa_K812032, BBa_K812110, BBa_K812130, BBa_K812132, BBa_K812133, BBa_K812200 and BBa_K812233.
- We designed a method for testing multicellular systems in Xenopus rapidly
- We provided 3 new plasmids for using this method, which include debugging tools
- We designed a multicellular hormonal system
- We created an Auxin production device for use in eukaryotes from the prokaryote one
- We submitted the Tir1 auxin detection device to the registry
- We showed the first Synthetic ecosystem, with a unicellular chassis (E.coli) improved theinside a multicellular chassis (Xenopus)
- We designed a new biobrick standard which allows one-shot coding device assembly, while still being compatible with the RFC10 standard
- We demonstrated it works (still with a low efficiency) and that the protocol have to be further optimized
- We managed to assemble parts with a very high efficiency using Golden Gate using the GoldenBricks plasmids
- We used a multi-level approach to approach a physiological system with a general integrative model in which we plugged data from more detailed models
- We sucessfully used Ordinary differential equations, partial differential equations and Guillespie Montecarlo algorithm to model detailed system in the tadpole
- We submitted an extensive report of our conclusions about synthetic biology in vertebrates, which is the fruit of our long reflection we conducted over the summer.