Team:Berkeley/Project/Construction

From 2012.igem.org

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We chose to use <a href="http://j5.jbei.org/j5manual/pages/23.html">Golden Gate Assembly</a> because it allowed us to either create single-pot libraries or the interchange of combinatorially expand the number of multi-gene devices with smaller constituent parts. Golden Gate (GG) is powered by Type IIs restriction enzymes, which cut distal to their recognition sites. Because of this, we have full control over the resulting 4bp overhangs, giving us a theoretical choice between 4^4, or 256 different overhangs. In practice, the set must be reduced to prevent misannealing.  
We chose to use <a href="http://j5.jbei.org/j5manual/pages/23.html">Golden Gate Assembly</a> because it allowed us to either create single-pot libraries or the interchange of combinatorially expand the number of multi-gene devices with smaller constituent parts. Golden Gate (GG) is powered by Type IIs restriction enzymes, which cut distal to their recognition sites. Because of this, we have full control over the resulting 4bp overhangs, giving us a theoretical choice between 4^4, or 256 different overhangs. In practice, the set must be reduced to prevent misannealing.  
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Revision as of 03:24, 2 October 2012

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iGEM Berkeley iGEMBerkeley iGEMBerkeley

Mercury

We chose to use Golden Gate Assembly because it allowed us to either create single-pot libraries or the interchange of combinatorially expand the number of multi-gene devices with smaller constituent parts. Golden Gate (GG) is powered by Type IIs restriction enzymes, which cut distal to their recognition sites. Because of this, we have full control over the resulting 4bp overhangs, giving us a theoretical choice between 4^4, or 256 different overhangs. In practice, the set must be reduced to prevent misannealing.


All about our MiCode design and cloning.