Difference between revisions of "Team:MIT"
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<img src="https://static.igem.org/mediawiki/2016/8/80/T--MIT--CascadeButton.svg" alt="Parts cascade" > | <img src="https://static.igem.org/mediawiki/2016/8/80/T--MIT--CascadeButton.svg" alt="Parts cascade" > | ||
| − | <span class="text-content"><span | + | <span class="text-content"><span><br><br><br><br><br><br><br>Read about a summary of our results and how our sensors interact logically after transfection of <br>4 to 5-unit genetic circuits into model cell cultures<br><br></span></span> |
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Revision as of 03:15, 17 October 2016
This diagnostic process can be expedited with synthetic biological tools that sense the following molecular markers in endometrial biopsy samples.
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Read more about how we created synthetic promoters to respond to this disease marker
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Read more about how we characterized miRNA profiles in model cells under varying conditions
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Read more about how we characterized serine integrase TP901 that could give a 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 more about the future of our work through circuit design and clinical application
