840:153g:Projects/project26/2012/10/04: Difference between revisions

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* On Tuesday we ran a gel on disgested and undigested snake DNA.  There were no significant bands of undigested DNA. We are going to try and change a few things like reducing our dilution buffer and adding more tissue. We are also going to run a PCR on the sample anyway.  On Thursday we started another extraction along with changes to the protocol.  
* On Tuesday we ran a gel on disgested and undigested snake DNA.  There were no significant bands of undigested DNA. We are going to try and change a few things like reducing our dilution buffer and adding more tissue. We are also going to run a PCR on the sample anyway.  On Thursday we started another extraction along with changes to the protocol.  


 
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Revision as of 12:44, 23 October 2012

Cloning of Atrolysin A <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
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DNA Extraction, Reconsitute Primers

  • On Tuesday we ran a gel on disgested and undigested snake DNA. There were no significant bands of undigested DNA. We are going to try and change a few things like reducing our dilution buffer and adding more tissue. We are also going to run a PCR on the sample anyway. On Thursday we started another extraction along with changes to the protocol.