Team:TPHS SanDiego/Project

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    <li><a href="https://2013hs.igem.org/Team:TPHS_SanDiego">Home  </a></li>
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        <a href="https://2013hs.igem.org/Team:TPHS_SanDiego/Project">Project</a>
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Our project focuses on promoter engineering. Our goal is to characterize a set of promoters (of our design) by moving the repressor and/or activator binding sites with respect to the -10 and -35 regions of the promoter. Ideally, we would like to show that by moving an activator binding site it can become a repressor and that by moving a repressor binding site it may become either irrelevant to transcription rate or even boost it. We also want to see if there is a steep decline in repressor/activator function as the binding site move along the promoter or if it is a gradual/linear change. We believe this project could have application to genetic circuits by allowing a single protein to either activate or repress a promoter depending on where the binding sites are placed on the promoter.
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<iframe src="https://docs.google.com/document/d/1epg-_5lpwccgvIzR7I_abmn-gJ08GCMvlULQiOUBI_A/pub?embedded=true" width="875" height="875" allowfullscreen="true" mozallowfullscreen="true" webkitallowfullscreen="true"></iframe></center><div class="row-end" ></div></center>
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Latest revision as of 23:21, 21 June 2013

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