Difference between revisions of "Team:Pittsburgh/Collaborations"
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| − | <h2 style="color: | + | <h2 style="color:#1c2957; padding-top:0;">Contents</h2> |
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<li><a href="#WM" class="table">William and Mary</a></li> | <li><a href="#WM" class="table">William and Mary</a></li> | ||
<li><a href="#UGA" class="table">University of Georgia</a></li> | <li><a href="#UGA" class="table">University of Georgia</a></li> | ||
| + | <li><a href="#surveys" class="table">Surveys</a></li> | ||
<li><a href="#UMD" class="table">Mid-Atlantic Meet-Up</a></li> | <li><a href="#UMD" class="table">Mid-Atlantic Meet-Up</a></li> | ||
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| + | <span class="anchor" id="WM"></span> | ||
| + | <h1>William and Mary: Circuit Control Toolbox</h1> | ||
| + | <p>The <a href="https://2016.igem.org/Team:William_and_Mary" target="_blank">William & Mary team</a> is developing a toolbox of parts that can be easily integrated into genetic circuits to tune the resulting levels of protein expression. They characterize their parts exclusively in <i>E. coli</i>. We tested eight of their toolbox parts in Promega's S30 Extract System for Circular DNA to compare the behavior of the parts in cells versus <i>in vitro</i>. The eight plasmids had different RBS strengths, which are reflected in our data shown below. Learn more about the experiments we performed and the results by reading our <a href="https://static.igem.org/mediawiki/2016/4/46/T--Pittsburgh--CollaborationsWM_report.pdf" target="_blank">report</a>.</p> | ||
| + | <img src="https://static.igem.org/mediawiki/2016/7/7c/T--Pittsburgh--CollaborationsWM_graph.jpg" alt="results" style="width:50%; display:block; margin:auto;"> | ||
| + | <a href="#Top">Back to Top</a> | ||
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| − | <span | + | <span class="anchor" id="UGA"></span> |
| + | <h1>University of Georgia: Archaeal InterLab</h1> | ||
| + | <p>The <a href="https://2016.igem.org/Team:UGA-Georgia" target="_blank">UGA team</a> is developing an mCherry library for <i>Methanococcus maripaludis</i>, an archaeal organism. Their library currently contains over 30 mutations in the RBS, which cause different levels of protein expression. We took fluorescence readings for several of these mutations as part of the "Archaeal InterLab." Like iGEM's InterLab Study, which aims to standardize fluorescence readings across all machines, the Archaeal InterLab recognizes that fluorescence lacks an absolute unit. Thus, participating teams record the relative fluorescence of the cells containing various RBS mutations for UGA.</p> | ||
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| + | <p>We were given five samples: three mutants (A, B, and C), a wild type (WT), and suspension buffer (S). Each of the samples was read in triplicate. Here are our average fluorescence readings for each sample. Error bars represent standard deviation. For more detailed protocols, notes, and data, visit our <a href="https://static.igem.org/mediawiki/2016/9/9f/T--Pittsburgh--NotebookWeek11.pdf" target="_blank"> Week 11 Lab Notebook</a>.</p> | ||
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| + | <img src="https://static.igem.org/mediawiki/2016/3/3f/T--Pittsburgh--CollaborationsUGAgraph.jpg" style="width:60%; display:block; margin: 0 auto;" alt="Results"> | ||
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| + | <span class="anchor" id="surveys"></span> | ||
| + | <div class="evry-badge"> | ||
| + | <a href="https://2016.igem.org/Team:Evry/HP" id="badge1" target="_blank"></a> | ||
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| + | <h1>Surveys</h1> | ||
| + | <p>Our team worked with team <a href="https://2016.igem.org/Team:Tianjin" target="_blank"> Tianjin</a> and other collaborators to create a survey about the use of synthetic biology to solve environmental problems. We also participated in surveys distributed by teams <a href="https://2016.igem.org/Team:Evry" target="_blank">Evry</a> and <a href="https://2016.igem.org/Team:LMU-TUM_Munich" target="_blank">Munich</a>. </p> | ||
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| + | <a href="#Top">Back to Top</a> | ||
| + | <span class="anchor" id="UMD"></span> | ||
| + | <h1 style="clear:both;">Mid-Atlantic Meet-Up</h1> | ||
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<p>On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, learning about other teams' projects, and discussing synthetic biology. They also explored College Park and the National Portrait Gallery in Washington D.C. with members of the UMaryland team. Thanks to the <a href="https://2016.igem.org/Team:UMaryland" target="_blank"> UMaryland team</a> for organizing such a great event and for being awesome hosts! Take a look at our presentation slides <a href="https://static.igem.org/mediawiki/2016/e/e9/T--Pittsburgh--CollabUMD.pdf" target="_blank">here</a>.</p> | <p>On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, learning about other teams' projects, and discussing synthetic biology. They also explored College Park and the National Portrait Gallery in Washington D.C. with members of the UMaryland team. Thanks to the <a href="https://2016.igem.org/Team:UMaryland" target="_blank"> UMaryland team</a> for organizing such a great event and for being awesome hosts! Take a look at our presentation slides <a href="https://static.igem.org/mediawiki/2016/e/e9/T--Pittsburgh--CollabUMD.pdf" target="_blank">here</a>.</p> | ||
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Latest revision as of 02:06, 19 October 2016
Contact Us
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Our work with other teams
William and Mary: Circuit Control Toolbox
The William & Mary team is developing a toolbox of parts that can be easily integrated into genetic circuits to tune the resulting levels of protein expression. They characterize their parts exclusively in E. coli. We tested eight of their toolbox parts in Promega's S30 Extract System for Circular DNA to compare the behavior of the parts in cells versus in vitro. The eight plasmids had different RBS strengths, which are reflected in our data shown below. Learn more about the experiments we performed and the results by reading our report.
Back to Top
University of Georgia: Archaeal InterLab
The UGA team is developing an mCherry library for Methanococcus maripaludis, an archaeal organism. Their library currently contains over 30 mutations in the RBS, which cause different levels of protein expression. We took fluorescence readings for several of these mutations as part of the "Archaeal InterLab." Like iGEM's InterLab Study, which aims to standardize fluorescence readings across all machines, the Archaeal InterLab recognizes that fluorescence lacks an absolute unit. Thus, participating teams record the relative fluorescence of the cells containing various RBS mutations for UGA.
We were given five samples: three mutants (A, B, and C), a wild type (WT), and suspension buffer (S). Each of the samples was read in triplicate. Here are our average fluorescence readings for each sample. Error bars represent standard deviation. For more detailed protocols, notes, and data, visit our Week 11 Lab Notebook.
Back to Top
Surveys
Our team worked with team Tianjin and other collaborators to create a survey about the use of synthetic biology to solve environmental problems. We also participated in surveys distributed by teams Evry and Munich.
Back to TopMid-Atlantic Meet-Up
On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, learning about other teams' projects, and discussing synthetic biology. They also explored College Park and the National Portrait Gallery in Washington D.C. with members of the UMaryland team. Thanks to the UMaryland team for organizing such a great event and for being awesome hosts! Take a look at our presentation slides here.
Back to Top