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Team:Cornell/Week 16
From 2011.igem.org
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==Tuesday, September 20== | ==Tuesday, September 20== | ||
| + | Afternoon lab work done by: Charlie Chung | ||
| + | :*VioA, VioB, and VioE plates = lots of bacterial colonies, high-density growth | ||
| + | ::- Picked three colonies from each plate and started up (3mL LB + 3µL carbenicillin) cultures | ||
| + | ::VioA-1,2,3 | ||
| + | ::VioB-1,2,3 | ||
| + | ::VioE-1,2,3 | ||
| + | :*RFP plate = ~5 colonies | ||
| + | ::- Picked two colonies and started up (3mL LB + 3µL carbenicillin) cultures | ||
| + | ::RFP-1,2 | ||
==Wednesday, September 21== | ==Wednesday, September 21== | ||
Revision as of 18:24, 20 September 2011
Week 1 | Week 2 - 5 | Week 6 | Week 7 | Week 8 | Week 9 | Week 10 | Week 11 | Week 12 | Week 13 | Week 14 | Week 15 | Week 16 | Week 17 | Week 18 | Week 19 | Week 20 | Week 21 |
September 18th - September 24th
Sunday, September 18
Monday, September 19
Morning lab work done by: Jim Mathew
- ...
Afternoon-1 lab work done by: Youjin Cho
- ...
Afternoon-2 lab work done by: Charlie Chung
- Background
- The PCR site-directed mutagenesis done earlier today should ideally enhance protein expression of VioA, VioB, VioE, and RFP by deleting excessive nucleotides between the ribosome binding site and the ATG start codon in the original DNA sequences
- Work Accomplished
- Plated the transformed products of VioA, VioB, VioE, and RFP on agar plates treated with ampicillin or carbenicillin (two are on amp; other two are on carb)
- Incubating at 37°C in Olin 303
Tuesday, September 20
Afternoon lab work done by: Charlie Chung
- VioA, VioB, and VioE plates = lots of bacterial colonies, high-density growth
- - Picked three colonies from each plate and started up (3mL LB + 3µL carbenicillin) cultures
- VioA-1,2,3
- VioB-1,2,3
- VioE-1,2,3
- RFP plate = ~5 colonies
- - Picked two colonies and started up (3mL LB + 3µL carbenicillin) cultures
- RFP-1,2
