Difference between revisions of "Team:MIT"
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<a href="https://2016.igem.org/Team:MIT/Description"> | <a href="https://2016.igem.org/Team:MIT/Description"> | ||
<img src="https://static.igem.org/mediawiki/2016/2/22/T--MIT--Homepage2Background2.svg" alt="Background" width="950px"> | <img src="https://static.igem.org/mediawiki/2016/2/22/T--MIT--Homepage2Background2.svg" alt="Background" width="950px"> | ||
| − | <span class="text-content"><span><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>Read more about endometriosis<br><br></span> | + | <span class="text-content"><span><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>Read more about endometriosis and our project design<br><br></span> |
</a> | </a> | ||
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<a href="https://2016.igem.org/Team:MIT/Experiments/miRNA"> | <a href="https://2016.igem.org/Team:MIT/Experiments/miRNA"> | ||
<img src="https://static.igem.org/mediawiki/2016/8/89/T--MIT--miRNAsensorsbutton.svg" alt="miRNA" > | <img src="https://static.igem.org/mediawiki/2016/8/89/T--MIT--miRNAsensorsbutton.svg" alt="miRNA" > | ||
| − | <span class="text-content"><span><br><br><br><br><br><br><br>We characterized | + | <span class="text-content"><span><br><br><br><br><br><br><br>We characterized microRNA profiles in model cells under varying conditions<br><br></span></span> |
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| − | + | <a href="https://2016.igem.org/Team:MIT/Attributions"> | |
| + | <img src="https://static.igem.org/mediawiki/2016/3/31/T--MIT--acknowledgments.svg"> | ||
| + | <span class="text-content"><span><br><br><br><br><br><br><br><br>Read more<br><br></span></span> | ||
| + | </a> | ||
</li> | </li> | ||
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Latest revision as of 19:05, 18 October 2016
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Read more about endometriosis and our project design
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We created new, synthetic promoters to respond to this disease marker
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We characterized microRNA profiles in model cells under varying conditions
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We characterized a serine integrase, TP901, that could give a genetic circuit memory across a cycle
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Read about a summary of our results and how our sensors interact logically after transfection of
4 to 5-unit genetic circuits into model cell cultures
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Read about how we worked with other iGEM teams throughout our project
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Read more about the future of our work through circuit design and clinical application
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Read more about our integrated human practices, mammalian synthetic biology toolbox, and public outreach
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Read more
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Read more
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Read more
