840:153g:Projects/project27/2012/11/01: Difference between revisions

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(Autocreate 2012/11/01 Entry for 840:153g:Projects/project27)
 
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==Entry title==
==Target Gene Amplification==
* Insert content here...
* Ran PCR reactions using ''M. trichosporium'' genomic DNA for template, 27F_mmoXY and 27R_mmoXY promoters to amplify XY gene segment, and 27F_mmoBZDC and 27R_mmoBZDC promoters to amplify BZDC gene segment. Each promoter pair was run at three different ligation temperatures, 55, 60, and 65.  The purpose of these reactions is to amplify the two target gene regions, adding biobricks, for insertion into plasmid vectors.  Next session, PCR products will be run on a gel to confirm lengths of amplified regions.
 


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Revision as of 13:14, 2 November 2012

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
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Target Gene Amplification

  • Ran PCR reactions using M. trichosporium genomic DNA for template, 27F_mmoXY and 27R_mmoXY promoters to amplify XY gene segment, and 27F_mmoBZDC and 27R_mmoBZDC promoters to amplify BZDC gene segment. Each promoter pair was run at three different ligation temperatures, 55, 60, and 65. The purpose of these reactions is to amplify the two target gene regions, adding biobricks, for insertion into plasmid vectors. Next session, PCR products will be run on a gel to confirm lengths of amplified regions.