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Team:Hawaii/Notebook/2008-10-22
From 2008.igem.org
| Projects | Events | Resources | ||
|---|---|---|---|---|
| Sponsors | Experiments | Milestones | Protocols | |
| Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Plasmid prep of BB-pRL1383a
- Grace
- E. coli did not grow. Reinoculated.
Extracted J04430 from filter paper
- Grace
- Used 2 μl of filter paper solution for PCR to verify plasmid
- Something is wrong with the J04430 filter spot iGEM sent us. PCR with VF2/VR primers did NOT yield the expected band ~1000bp.
Transformation
- Grace
- Used 2 μl each of BBpRL1383a-1 and J04430 (from filter) to transform DB3.1
Construction of GFP secretion device
- Krystle
- Gel purify restriction digests from yesterday
- Ligate nir+rbs and slr+gfpf into restricted psB1A3 from Margaret
- Transformed into DH5α
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 
]
