Team:Calgary/23 June 2009
From 2009.igem.org
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* The isolated plasmid was pooled together and attempted to concentrate the plasmid by spinning the tube in a vacifuge. After several hours (2.5 hours) the concentration was higher. | * The isolated plasmid was pooled together and attempted to concentrate the plasmid by spinning the tube in a vacifuge. After several hours (2.5 hours) the concentration was higher. | ||
* Tried ethanol precipitation earlier in the day but there was no precipitate found when done. | * Tried ethanol precipitation earlier in the day but there was no precipitate found when done. | ||
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*Objective: To do one last verification that LuxOD47E is in the psB1AC3 vector before we send it down for DNA Sequecning. We will do a NotI digest with | *Objective: To do one last verification that LuxOD47E is in the psB1AC3 vector before we send it down for DNA Sequecning. We will do a NotI digest with | ||
- | *Started with Plasmid | + | *Started with Plasmid Isolation this morning (Sigma). |
*Used 1000 Nanodrop Spectrophotometer to determine concentrations. | *Used 1000 Nanodrop Spectrophotometer to determine concentrations. | ||
*Set up a restriction digest with NotI enzyme and REact Buffer 3, left to digest in the 37 C waterbath overnight. | *Set up a restriction digest with NotI enzyme and REact Buffer 3, left to digest in the 37 C waterbath overnight. |
Latest revision as of 06:26, 20 October 2009
UNIVERSITY OF CALGARY