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<a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Description">Description</a> | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Description">Description</a> | ||
<a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Design">Design</a> | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Design">Design</a> | ||
+ | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Model">Model</a> | ||
+ | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/InterLab">InterLab</a> | ||
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− | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/ | + | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Notebook">Notebook</a> |
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<a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Integrated_Practices">Integrated | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Integrated_Practices">Integrated | ||
Practices</a> | Practices</a> | ||
+ | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Public_Engagement">Public | ||
+ | Engagement</a> | ||
<a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Collaborations">Collaborations</a> | <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Collaborations">Collaborations</a> | ||
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<h2 align="center">InterLab</h2> | <h2 align="center">InterLab</h2> | ||
+ | <p>For this year’s InterLab study, we performed bacterial transformations in E. Coli using the plasmids | ||
+ | provided by iGEM. These plasmids had different levels of fluorescence, which was validated using a cell | ||
+ | plate reader that measured absorbance as well as fluorescence. A range of fluorescence was observed in the | ||
+ | different plasmids, some having a level of fluorescence as low as the negative control and others having a | ||
+ | level of fluorescence as high as the positive control. The InterLab protocol that was provided was | ||
+ | straightforward and easy to follow. The diagrams that were provided illustrating the experimental designs | ||
+ | were very helpful and all these factors contributed to an overall positive experience. | ||
+ | </p> | ||
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<a href="https://static.igem.org/mediawiki/2018/f/f0/T--New_York_City--InterLab.xlsx"> | <a href="https://static.igem.org/mediawiki/2018/f/f0/T--New_York_City--InterLab.xlsx"> | ||
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− | <a href="https://twitter.com/HDNYC_iGEM">< | + | <a href="https://twitter.com/HDNYC_iGEM"><img class="social" src="https://static.igem.org/mediawiki/2018/4/46/T--New_York_City--twit.png"></a> |
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− | <a href="https://www.instagram.com/nyc_igem/">< | + | <a href="https://www.instagram.com/nyc_igem/"><img class="social" src="https://static.igem.org/mediawiki/2018/0/0a/T--New_York_City--ig.png"></a> |
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Latest revision as of 01:38, 17 October 2018
InterLab
For this year’s InterLab study, we performed bacterial transformations in E. Coli using the plasmids provided by iGEM. These plasmids had different levels of fluorescence, which was validated using a cell plate reader that measured absorbance as well as fluorescence. A range of fluorescence was observed in the different plasmids, some having a level of fluorescence as low as the negative control and others having a level of fluorescence as high as the positive control. The InterLab protocol that was provided was straightforward and easy to follow. The diagrams that were provided illustrating the experimental designs were very helpful and all these factors contributed to an overall positive experience.