Team:IIT Madras/Dry lab/Tools

From 2011.igem.org

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<p align="center"><img src="https://static.igem.org/mediawiki/2011/1/17/Tool-3.jpg" width="800" height="600"/></p><br/>
<p align="center"><img src="https://static.igem.org/mediawiki/2011/1/17/Tool-3.jpg" width="800" height="600"/></p><br/>
<p align="center"><b> <u>Fig(3): Showing The Output of the toolbox </u></b><br/><br/><br/>
<p align="center"><b> <u>Fig(3): Showing The Output of the toolbox </u></b><br/><br/><br/>
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<p> The novelty here is that the complete protein sequence and all the sites at which a <b>specific mutation</b> is required can be given at a time. This would generate the best possible <b>primers</b> required also accounting for distance between the mutations hence optimizing the number of primers.
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Revision as of 03:06, 6 October 2011

bar iGEM 2011 - Home Page Indian Institute of Technology - Madras








Site directed Mutagenesis-Primer Design

We received proteorhodopsin sequence from Kwang-Hwan "Kevin" Jung, Ph.D., Associate Professor, Department of Life Science and Institute of Biological Interfaces, Sogang University with three restriction sites EcoRI, SpeI and PstI. Hence the plasmid had to be mutated for iGEM compatibility. Hence we had to design primers for site directed mutagenesis at each of these sites. So we have come up with a Primer design tool for SDM as a Criteria:

  1. Mutations in the middle of primer
  2. Tm difference should be less than 5
  3. No 3' Breathing should be ensured by keeping G or C at the end
  4. GC content:40-60%

Fig(1): Showing The Command Prompt


Fig(2): Showing The Output of the toolbox



Fig(3): Showing The Output of the toolbox


The novelty here is that the complete protein sequence and all the sites at which a specific mutation is required can be given at a time. This would generate the best possible primers required also accounting for distance between the mutations hence optimizing the number of primers.