Line 99: | Line 99: | ||
<h2 style="color:rgb(0.0.128); padding-top:0;">Contents</h2> | <h2 style="color:rgb(0.0.128); padding-top:0;">Contents</h2> | ||
<ul class="table"> | <ul class="table"> | ||
− | + | ||
<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="#WM" class="table">William and Mary</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> | ||
</ul> | </ul> | ||
Line 106: | Line 107: | ||
<div class="notebook column full_size"> | <div class="notebook column full_size"> | ||
+ | |||
+ | <span clas="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> | ||
+ | <a href="#Top">Back to Top</a> | ||
− | <span clas="anchor" id=" | + | <span clas="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 their toolbox parts in a cell extract system to compare the behavior of the parts in cells versus <i>in vitro</i>.</p> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <span clas="anchor" id="UMD"></span> | ||
+ | <!--IMAGE GALLERY START--> | ||
<div style="float:right;width:40%;"> | <div style="float:right;width:40%;"> | ||
<div class="slideshow-container"> | <div class="slideshow-container"> | ||
Line 162: | Line 174: | ||
</div> | </div> | ||
</div> | </div> | ||
+ | <!--IMAGE GALLERY END--> | ||
<h1>Mid-Atlantic Meet-Up</h1> | <h1>Mid-Atlantic Meet-Up</h1> |
Revision as of 00:20, 3 August 2016
Contact Us
Our work with other teams
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.
Back to TopWilliam 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 their toolbox parts in a cell extract system to compare the behavior of the parts in cells versus in vitro.
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