Team:Peking R
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<div class="VISITORSFROM" id="apDiv17"><a href="https://2011.igem.org/Team:Peking_S"><img src="https://static.igem.org/mediawiki/2011/7/71/Peking_R_links_to_Peking_S.png" width="164" height="58" /></a></div> | <div class="VISITORSFROM" id="apDiv17"><a href="https://2011.igem.org/Team:Peking_S"><img src="https://static.igem.org/mediawiki/2011/7/71/Peking_R_links_to_Peking_S.png" width="164" height="58" /></a></div> | ||
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Revision as of 10:34, 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. |
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