Team:Peking R
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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> | <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/Parts"><img src="https://static.igem.org/mediawiki/2011/5/5f/PekingR_parts_smallpicture.png" width="304" height=" | + | <th scope="col"><a href="https://2011.igem.org/Team:Peking_R/Parts"><img src="https://static.igem.org/mediawiki/2011/5/5f/PekingR_parts_smallpicture.png" width="304" height="187" /></a></th> |
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- | <div id="apDiv12"><a href="https://2011.igem.org/Team:Peking_R/Biosafety/zmq"><img src="https://static.igem.org/mediawiki/2011/3/3c/PekingR_biosafety2.3.png" width=" | + | <div id="apDiv12"><a href="https://2011.igem.org/Team:Peking_R/Biosafety/zmq"><img src="https://static.igem.org/mediawiki/2011/3/3c/PekingR_biosafety2.3.png" width="208" height="27" /></a> |
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Revision as of 10:33, 3 October 2011
Template:Https://2011.igem.org/Team:Peking R/bannerhidden Template:Https://2011.igem.org/Team:Peking R/back2 Template:Https://2011.igem.org/Team:Peking R/homepagebanner
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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