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Team:Hawaii/Notebook/2008-08-11
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(New page: {{Team:Hawaii/Header}} = Things we did today = == Wetlab work == ===Checked plasmid prep from weekend=== :<strong> Grace</strong> [[Image:081108plasmidprep.jpg|right|thumb|200px|EtBr stai...)
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(New page: {{Team:Hawaii/Header}} = Things we did today = == Wetlab work == ===Checked plasmid prep from weekend=== :<strong> Grace</strong> [[Image:081108plasmidprep.jpg|right|thumb|200px|EtBr stai...)
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Revision as of 23:36, 11 August 2008
| Projects | Events | Resources | ||
|---|---|---|---|---|
| Sponsors | Experiments | Milestones | Protocols | |
| Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Checked plasmid prep from weekend
- Grace
[[Image:081108plasmidprep.jpg|right|thumb|200px|EtBr stained 0.8% agarose gel ran at 95V for 1 hour. Five microliters of plasmid were loaded into each well.
- Ran on 2.0% agarose gel to verify plasmids
- DNA didn't run. Agarose concentration too high. Redid on 0.8% gel.
- Genomic DNA up top?
- Clean prep (no RNA)!
- Only E0240 verified. All other bands wrong size (circular/supercoiled?)
- Checked DNA concentrations via nanodrop spectrometer
| Plasmid | DNA concentration | 260/280 | 260/230 |
|---|---|---|---|
| E0240 | 757.7 ng/μl | 2/06 | 1.49 |
| I14032 (2005 distribution) | 541.4 ng/μl | 2.01 | 1.27 |
| I51020 | 2775.6 ng/μl | 1.97 | 1.77 |
| nir+rbs | 566.8 ng/μl | 1.83 | 1.10 |
| plac+rbs | 344.0 ng/μl | 1.95 | 1.28 |
Made 1000x Amp,sub>100</sub> stock solution
- Grace
Reinoculated for cryostocking
- Grace
- I14032 from 2005 and 2008 distributions
Construction of GFP device
- Grace
- Extracted nir+rbs, plac+rbs, GFP, GFPf from gel ran yesterday
- B0015 could not be extracted because fragment was not visible under short wave UV
- Digestion was done for 3A assembly rather than rear ligation (oops). Redid RE digest.
- Checked DNA concentrations via nanodrop spectrometer
| Part | DNA concentration | _ | nir+rbs | 4.8 ng/μl |
|---|---|---|---|---|
| plac+rbs | 3.6 ng/μl | |||
| GFP | 4.7 ng/μl | |||
| GFPfusion | 6.4 ng/μl |
- Restriction digested in 30 μl reactions:
- B0015 with XbaI then EcoRI
- GFP and GFPf with EcoRI and SpeI
- slr1, slr2, pilA with SpeI and PstI
- Ran new RE digests EtBr stained 2% agarose gel at 72V for 2 hours
- Extracted parts from gel and determined DNA concentrations
Discussion
- FYI:
- According to the Endy lab, ligation reactions should have <100ng DNA per reaction for maximum efficiency
- ~10ng vector should be used in ligation reactions (6:1 ratio of insert to vector)
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 
]
