Team:Peking R

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<div id="apDiv19"><img src="https://static.igem.org/mediawiki/2011/7/79/Pekingr2-1.gif" width="157" height="124">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<img src="https://static.igem.org/mediawiki/2011/7/79/Pekingr2-2.gif" width="182" height="117"> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<img src="https://static.igem.org/mediawiki/2011/e/ec/Pekingr2-3.gif" width="227" height="92"></div>
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<div id="apDiv19"><img src="https://static.igem.org/mediawiki/2011/7/79/Pekingr2-1.gif" width="157" height="124">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<img src="http://www.chem.pku.edu.cn/chenpeng/igem/images/igem.png" width="150" height="115"> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<img src="https://static.igem.org/mediawiki/2011/e/ec/Pekingr2-3.gif" width="227" height="92"></div>
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Revision as of 12:00, 3 October 2011

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In our project, we aim at establishing an extensible and versatile platform for the softcoding of genetic program in bacteria, composed of a toolbox and a methodology. The toolbox consists of interoperable and truly modular ligand-responsive riboswitches/ribozymes, while the methodology is automated design of synthetic ribosome binding sites (RBS) with customized translation rate. When combining them together, a quantitative correlation between the concentration of specific ligand and synthetic RBS strength can be established. To learn more, please click here.