Team:Peking R

From 2011.igem.org

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       <th width="277" bgcolor="#FFFFFF" scope="col"><a href="https://2011.igem.org/Team:Peking_R/Project/RBSAutomatedDesign"><img src="https://static.igem.org/mediawiki/2011/2/24/PekingR_project1.png" width="200" height="150" border="0" /></a></th>
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       <th width="257" bgcolor="#FFFFFF" scope="col"><a href="https://2011.igem.org/Team:Peking_R/Project/RNAToolkit">  <img src="https://static.igem.org/mediawiki/2011/f/fc/PekngR_project3.png" width="150" height="150" /></a></th>
       <th width="257" bgcolor="#FFFFFF" scope="col"><a href="https://2011.igem.org/Team:Peking_R/Project/RNAToolkit">  <img src="https://static.igem.org/mediawiki/2011/f/fc/PekngR_project3.png" width="150" height="150" /></a></th>
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       <th scope="col"><a href="https://2011.igem.org/Team:Peking_R/Team/Gallery"><img src="https://static.igem.org/mediawiki/2011/1/12/PpekingR_biosafety_smallpicture.png" width="226" height="150" /></a></th>
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Revision as of 12:07, 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.