Team:Hawaii/Notebook/2008-08-20
From 2008.igem.org
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:*These annealed products can be found in the -20°C freezer in the DNA box. | :*These annealed products can be found in the -20°C freezer in the DNA box. | ||
:*Quantification was achieved simply by adding up the amount of DNA added. | :*Quantification was achieved simply by adding up the amount of DNA added. | ||
+ | ::* plac (I14032) for front ligation --> 370ng/ul | ||
+ | ::* rbs 1.0 (B0034) for back ligation --> 206.7ng/ul | ||
+ | ::* rbs 0.6 (B0030) for front ligation --> | ||
+ | ::* tt (B1006) for back ligation --> 375ng/ul | ||
Revision as of 03:07, 23 August 2008
Projects | Events | Resources | ||
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Sponsors | Experiments | Milestones | Protocols | |
Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Name of Task
- Margaret & Krystle
- Annealed and phosphorylated:
- plac (I14032) for front ligation
- rbs 1.0 (B0034) for back ligation
- rbs 0.6 (B0030) for front ligation
- tt (B1006) for back ligation
- We decided to perform this reaction again with out gel purification and the gel was discarded.
- These annealed products can be found in the -20°C freezer in the DNA box.
- Quantification was achieved simply by adding up the amount of DNA added.
- plac (I14032) for front ligation --> 370ng/ul
- rbs 1.0 (B0034) for back ligation --> 206.7ng/ul
- rbs 0.6 (B0030) for front ligation -->
- tt (B1006) for back ligation --> 375ng/ul
Discussion
Quote of the Day
History is the only laboratory we have in which to test the consequences of thought. - Étienne Gilson
[http://manoa.hawaii.edu/ ][http://manoa.hawaii.edu/ovcrge/ ][http://www.ctahr.hawaii.edu ]