User:Elaine Marie Robbins/Notebook/CHEM-496/2011/09/21: Difference between revisions
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<center>[[image:DNA gel 092111 003.jpg]]</center> | <center>[[image:DNA gel 092111 003.jpg]]</center> | ||
The ladder | The first column is the ladder. The next columns are groups 1, 2, 3, 4, and 5. | ||
==Notes== | ==Notes== |
Revision as of 12:07, 4 October 2011
Gel Electrophoresis of PCR Product | <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> |
ObjectiveTo determine whether or not the PCR performed on 09/20/11 of the DNA coding for a mutant GFP was successful using agarose gel electrophoresis. Description
DataA photo of the electrophoresis gel is displayed below: The first column is the ladder. The next columns are groups 1, 2, 3, 4, and 5. NotesGel ladder: 500 bp, 1000 bp, 2000 bp, 3000 bp, 4000 bp, 5000 bp, 6000 bp, 7000 bp, 8000 bp, 9000 bp, 10000 bp An optimum gel would have used 1.5% agarose.
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