Wisconsin: Lignin Project/17 June 2008

From 2008.igem.org

(Difference between revisions)
(New page: '''Team Fungus:''' <br> Received primers <br> Diluted primers <br> Ran TAQ PCR reaction with Carbon-limited cDNA <br> Ran PCR product on 1% agrose gel; only ladder visible <br>)
 
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{|align="justify" style="color:#aada84;background-color:#000;" width="800 px"
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|'''Team Sorbitol:'''
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Harvested the chromosomal DNA from the overnight MG1655 cultures by boiling the cells.<br>
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Used this DNA as a template for 2 PCR reactions.<br>
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One reaction was to clone out ''srlD'' the other was to clone the ''srl'' operon.<br>
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However when run on a gel no bands were found.<br>
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'''Team Fungus:''' <br>
'''Team Fungus:''' <br>
Received primers <br>
Received primers <br>
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Ran TAQ PCR reaction with Carbon-limited cDNA <br>
Ran TAQ PCR reaction with Carbon-limited cDNA <br>
Ran PCR product on 1% agrose gel; only ladder visible <br>
Ran PCR product on 1% agrose gel; only ladder visible <br>
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|}

Latest revision as of 15:15, 8 August 2008

Igemwibanner.gif
Team Sorbitol:

Harvested the chromosomal DNA from the overnight MG1655 cultures by boiling the cells.
Used this DNA as a template for 2 PCR reactions.
One reaction was to clone out srlD the other was to clone the srl operon.
However when run on a gel no bands were found.

Team Fungus:
Received primers
Diluted primers
Ran TAQ PCR reaction with Carbon-limited cDNA
Ran PCR product on 1% agrose gel; only ladder visible