From 2008.igem.org
Things we did today
Wetlab work
Checked plasmid prep from weekend
- Grace
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
-
- 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 
]
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