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Team:Hawaii/Notebook/2008-07-29
From 2008.igem.org
| Projects | Events | Resources | ||
|---|---|---|---|---|
| Sponsors | Experiments | Milestones | Protocols | |
| Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Gel purification of ccdB PCR product
- Grace
RE digests
- Grace
- Digested pRL1383a (from last night) with BamHI
- Digested B0030 and B0024 (from last night) with EcoRI
- Sequentially digested gel purified ccdB with HindIII and BamHI
Construction of BioBricks
- Grace
- Purified RE digests on EtBr stained 3% agarose gel
- Extracted bands for B0030 and B0024
- Other lanes FAILED!
Direct Band Extraction Method
- make two comb gels
- run test UPA band along with ladder
- attempt to pipette out DNA as it runs into the second well
- no more gel cutting???
PCR amplification of pRL1383a parts
- Margaret
- Made a reaction buffer containing {38.5ul, 20ul accusure, 10ul dNTPs, & 5ul 5XBuffer}. This should be good for 20 50ul reactions.
- Amplified with Accusure: aadA ([http://partsregistry.org/Part:BBa_J23012 BBa_J23012]), aadaA (pRL1383a), rep region, oriV
- Amplified with Green Taq: rep region
Media
- started to make LB amp100 plates, but autoclave room is closed. Remember to do it tomorrow.
Discussion
- SYBR Safe
- Blue light still doesn't illuminate the bands well. No bands (not even the ladder) are visible. Resolution *much* better with short wave UV. EtBr better bet for now?
- Restriction enzymes
- HindIII and BamHI in the lab -20C freezer (in box labeled "TKW Restriction Enzymes") fail. They're really old and don't appear to cut well anymore. Digestion of pRL1383a resulted in a long smear.
Quote of the Day
LOL! http://www.youtube.com/watch?v=J0s0Y3-BCaw
