Team:Alberta/Parts

From 2013.igem.org

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       <p> An important aspect of the iGEM competition is the use and creation of standard  biological parts. Each team will make new parts during iGEM and will place them in the [http://partsregistry.org Registry of Standard Biological Parts]. The iGEM software provides an easy way to present the parts your team has created . The "groupparts" tag will generate a table with all of the parts that your team adds to your team sandbox.  Note that if you want to document a part you need to document it on the [http://partsregistry.org Registry], not on your team wiki.
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       <p> Our 2013 parts submitted are a set of violacein genes derived from the violacein operon constructed and          
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        submitted by Cambridge in 2009 (BBa_K274002). We have made a number of modifications, including upgrading the      
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Remember that the goal of proper part documentation is to describe and define a part such that it can be used without a need to refer to the primary literature. The next iGEM team should be able to read your documentation and be able to use the part successfully. Also, you should provide proper references to acknowledge previous authors and to provide for  users who wish to know more.</p>
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        plasmid backbone from pSB1K3 to pSB1C3 standard 10, and converting each of the five open reading frames into       
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        its own part with a common and improved ribosome binding site (BBa_B0030) such that they can be assembled in       
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        different combinations and permutations. All of the parts have been characterized and are functional, and we       
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        have found that a new combination, VioABCE, produces a new pigment which we call "Royal Blue". </p>
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<groupparts>iGEM013 Alberta</groupparts>
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  <groupparts>iGEM013 Alberta</groupparts>
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Revision as of 17:50, 26 September 2013

The Littlest Mapmaker

"Exploration into the world of DNA Computing"
Team Alberta: University of Alberta

BioBricks

Our 2013 parts submitted are a set of violacein genes derived from the violacein operon constructed and submitted by Cambridge in 2009 (BBa_K274002). We have made a number of modifications, including upgrading the plasmid backbone from pSB1K3 to pSB1C3 standard 10, and converting each of the five open reading frames into its own part with a common and improved ribosome binding site (BBa_B0030) such that they can be assembled in different combinations and permutations. All of the parts have been characterized and are functional, and we have found that a new combination, VioABCE, produces a new pigment which we call "Royal Blue".

 <groupparts>iGEM013 Alberta</groupparts>