Team:CU-Boulder/Project

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<dt>The 2013 CU-Boulder iGEM Project</dt>
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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<p>The main focus of the iGEM project here at CU-Boulder is to help make synthetic biology more accessible and affordable.  We spent the summer developing parts, procedures, and documentation to help make this vision a reality.  The original goal was to create the constructs and purification methods necessary to produce and isolate restriction enzymes. Along the way we explored some novel approaches to DNA and protein purification and developed experimentally tested protocols for these and other procedures essential to Biobrick assembly.  Our purification methods exemplify the ideal of using common lab materials to make performing everyday lab techniques as accessible and inexpensive as possible.  A related aspect of our project was exploring methods of recycling consumables associated with lab work in order to reduce waste and material expenses.  We hope that our findings using this "do-it-yourself" approach of synthetic biology help make this type of research more accessible for those where funding is a limiting factor.
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<li><a href="https://2013.igem.org/Team:CU-Boulder/Project/Kit/RestrictionEnzymes">Restriction Enzymes</a></li>
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<li><a href="https://2013.igem.org/Team:CU-Boulder/Project/Kit/Purification">Protein Purification</a></li>
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<li><a href="https://2013.igem.org/Team:CU-Boulder/Project/Kit/DNAPurification">DNA Purification</a></li>
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
 
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!align="center"|[[Team:CU-Boulder|Home]]
 
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!align="center"|[[Team:CU-Boulder/Team|Team]]
 
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=CU-Boulder Official Team Profile]
 
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!align="center"|[[Team:CU-Boulder/Project|Project]]
 
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!align="center"|[[Team:CU-Boulder/Parts|Parts Submitted to the Registry]]
 
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!align="center"|[[Team:CU-Boulder/Modeling|Modeling]]
 
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!align="center"|[[Team:CU-Boulder/Notebook|Notebook]]
 
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!align="center"|[[Team:CU-Boulder/Safety|Safety]]
 
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Restriction Enzymes are necessary tools in synthetic biology, without them, biobrick assembly would be impossible. These restriction enzymes are also very pricey and prove to be a significant cost in labs everywhere. Because these enzymes are expensive, but necessary, experiments in synthetic biology are limited to companies and universities with high budgets. Here at the University of Colorado-Boulder, we aim to find a technology that lowers the costs of these restriction enzymes and open the field of synthetic biology to more people.
 
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Our solution to this problem we are trying to create is a "BetaBioBrick." Essentially we are trying to come up a with low cost method for labs to create their own restriction enzymes so they won't have to order from pricey suppliers. We attempting to do this by creating a BioBrick part that will house the genes for a restriction enzyme (EcoRI, XbaI, ApoI), their relative methylase, and if needed a method of purification.
 
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== Project Details==
 
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=== Part 2 ===
 
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=== The Experiments ===
 
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=== Part 3 ===
 
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== Results ==
 

Latest revision as of 15:35, 28 October 2013

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The 2013 CU-Boulder iGEM Project

The main focus of the iGEM project here at CU-Boulder is to help make synthetic biology more accessible and affordable. We spent the summer developing parts, procedures, and documentation to help make this vision a reality. The original goal was to create the constructs and purification methods necessary to produce and isolate restriction enzymes. Along the way we explored some novel approaches to DNA and protein purification and developed experimentally tested protocols for these and other procedures essential to Biobrick assembly. Our purification methods exemplify the ideal of using common lab materials to make performing everyday lab techniques as accessible and inexpensive as possible. A related aspect of our project was exploring methods of recycling consumables associated with lab work in order to reduce waste and material expenses. We hope that our findings using this "do-it-yourself" approach of synthetic biology help make this type of research more accessible for those where funding is a limiting factor.

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