Wisconsin: Lignin Project/23 June 2008

From 2008.igem.org

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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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Decided to use Herculase instead of TAQ in the PCR reactions (Herculase has proofreading ablitity)<br>
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Ran a new PCR reaction using the specific volumes designated by the Herculase designers.<br>
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No Bands formed.<br>
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'''Team Fungus:''' <br>
'''Team Fungus:''' <br>
Ran a touchdown PCR of Carbon and Nitrogen-limited cDNA using Herculase II polymerase<br>
Ran a touchdown PCR of Carbon and Nitrogen-limited cDNA using Herculase II polymerase<br>
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Ran PCR products through 0.9% agrose gel at 100V<br>
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Ran PCR products through 0.9% agrose gel at 100V: bands present for both at about 1.1kb <br>
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-Bands present for both at about 1.1kb <br>
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Grew overnight culture of pET28a <br>
Grew overnight culture of pET28a <br>
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'''Team Sorbitol:'''<br>
 

Latest revision as of 15:21, 8 August 2008

Igemwibanner.gif
Team Sorbitol:

Decided to use Herculase instead of TAQ in the PCR reactions (Herculase has proofreading ablitity)
Ran a new PCR reaction using the specific volumes designated by the Herculase designers.
No Bands formed.

Team Fungus:
Ran a touchdown PCR of Carbon and Nitrogen-limited cDNA using Herculase II polymerase
Ran PCR products through 0.9% agrose gel at 100V: bands present for both at about 1.1kb

Grew overnight culture of pET28a