Minnesota/25 July 2008
From 2008.igem.org
(Difference between revisions)
Emartin9808 (Talk | contribs) (New page: {|style="align:left" width="965" |- |''' Back to Notebook Home''' |- |'''Go to Previous Day (July 24)'''|| width=158|'''[[...) |
Emartin9808 (Talk | contribs) |
||
Line 9: | Line 9: | ||
|- | |- | ||
|'''1. No growth on plates:''' Experiments on 07-24-08 failed to show growth on Kanamycin resistant plates. | |'''1. No growth on plates:''' Experiments on 07-24-08 failed to show growth on Kanamycin resistant plates. | ||
+ | |- | ||
+ | |'''2. Redoing ligation:''' Using left over double digest from 07-24-08, But increase the amount of ligase in the reaction and performing the ligations @ 60C which is the optimal temperature for the ligase. | ||
+ | |- | ||
+ | |'''3. Redoing transformations:''' Redo with new ligated products by adding much less DNA/plasmid to the TOP10 Cells, b/c if put too much ligated DNA then the cells do not transform properly (as stated by iGEM troubleshooting). |
Revision as of 15:09, 25 July 2008
Back to Notebook Home | |
Go to Previous Day (July 24) | Go to Next Day (July 28) |
1. No growth on plates: Experiments on 07-24-08 failed to show growth on Kanamycin resistant plates. |
2. Redoing ligation: Using left over double digest from 07-24-08, But increase the amount of ligase in the reaction and performing the ligations @ 60C which is the optimal temperature for the ligase. |
3. Redoing transformations: Redo with new ligated products by adding much less DNA/plasmid to the TOP10 Cells, b/c if put too much ligated DNA then the cells do not transform properly (as stated by iGEM troubleshooting). |