840:153g:Projects/project22/2012/10/04: Difference between revisions
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[http://openwetware.org/images/thumb/4/44/%21GROUP22.25O.tif/640px-%21GROUP22.25O.tif.png] | [http://openwetware.org/images/thumb/4/44/%21GROUP22.25O.tif/640px-%21GROUP22.25O.tif.png] | ||
Wells 18-20 were ours (negative controls, far left side) | Wells 18-20 were ours (negative controls and marker, far left side) | ||
[http://openwetware.org/images/thumb/e/ef/%21GROUP24.2.tif/640px-%21GROUP24.2.tif.png] | [http://openwetware.org/images/thumb/e/ef/%21GROUP24.2.tif/640px-%21GROUP24.2.tif.png] | ||
Revision as of 15:29, 4 October 2012
 Prodigiosin Production by E. Coli.
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<html><img src="/images/9/94/Report.png" border="0" /></html> Main project page <html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html> </html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html> |
PCR Results and RetryOn Tuesday we ran simple gel electrophoresis of our PCR products. Unfortunately, our DNA's signal was very weak and the positive control failed as well. Today we attempted to concentrate the DNA in our samples in a Speed Vacuum Concentrator and will run PCR on this DNA to check said concentration. If the DNA is sufficiently concentrated, we will take another shot at PCR. We will first retest the positive control with a few of our primers to make sure the controls work properly before we go all in. Wells 1-12 were ours (markers at 5 and 12 going right to left) [1] Wells 18-20 were ours (negative controls and marker, far left side) [2] | |
![[1]](http://openwetware.org/images/thumb/4/44/%21GROUP22.25O.tif/640px-%21GROUP22.25O.tif.png){kind=link}
![[2]](http://openwetware.org/images/thumb/e/ef/%21GROUP24.2.tif/640px-%21GROUP24.2.tif.png){kind=link}