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Team:Peking R
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| - | <th width="277" bgcolor="#FFFFFF" scope="col"><img src="http://www.chem.pku.edu.cn/chenpeng/igem/images/tpp aptamer.png" width=" | + | <th width="277" bgcolor="#FFFFFF" scope="col"><img src="http://www.chem.pku.edu.cn/chenpeng/igem/images/tpp aptamer.png" width="214" height="150"></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> | ||
Revision as of 12:12, 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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