840:153g:Projects/project13/2010/11/11: Difference between revisions
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* Thursday we repeated the gel. We put in 12 μL of DNA in our mixtures for our ligated part. So we could get a more vivid representation of our DNA fragments. We cut our our ligated part with Ecori and Spel. | * Thursday we repeated the gel. We put in 12 μL of DNA in our mixtures for our ligated part. So we could get a more vivid representation of our DNA fragments. We cut our our ligated part with Ecori and Spel. We think that cultures 11-13 might have worked but the rest of the cultures did not appear to be cut. | ||
* We also are running a gel for part BBa_J23102. We potentially want to use this as a plasmid for our ligated part. We are checking to make sure that the plasmid part can be cut out out of the vector backbone. | * We also are running a gel for part BBa_J23102. We potentially want to use this as a plasmid for our ligated part. We are checking to make sure that the plasmid part can be cut out out of the vector backbone. | ||
Revision as of 15:24, 11 November 2010
- Tuesday we ran an electrophorysis gel and it was either not completely soldified or the agar was not completely dissovled before pouring because our gel was shriveled and could not be analyzed.
- Thursday we repeated the gel. We put in 12 μL of DNA in our mixtures for our ligated part. So we could get a more vivid representation of our DNA fragments. We cut our our ligated part with Ecori and Spel. We think that cultures 11-13 might have worked but the rest of the cultures did not appear to be cut.
- We also are running a gel for part BBa_J23102. We potentially want to use this as a plasmid for our ligated part. We are checking to make sure that the plasmid part can be cut out out of the vector backbone.
