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Team:Cornell/Week 16
From 2011.igem.org
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==Saturday, September 24== | ==Saturday, September 24== | ||
| - | + | Microfluidics work done by: Maneesh Gupta | |
| - | + | :*... | |
| + | Lab work done by: Jim Mathew, Nancy Li, Charlie Chung, Claire Paduano | ||
| + | :*PCR | ||
Revision as of 20:17, 24 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
Lab work done by: Jim Mathew, Youjin Cho, 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
- PCR procedure for deletion technique
- Using 1µl of PCR product of VioA, VioB, VioE and RFP, transformed them into DH5α electrocompetent cells via electroporation
- Put the transformed samples in 37°C shaker for an hour
- 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
- - Incubating at 37°C in Olin 304
- RFP plate = ~5 colonies
- - Picked two colonies and started up (3mL LB + 3µL carbenicillin) cultures
- RFP-1,2
- - Incubating at 37°C in Olin 304
Wednesday, September 21
Morning lab work done by: Charlie Chung
- Transferred 500µL from each culture tube to 20mL (LB + carbenicillin) subcultures
- - Shaking at 37°C in Olin 304
- Miniprep the remaining cultures of VioA-1,2,3 ; VioB-1,2,3 ; VioE-1,2,3 ; RFP-1,2
- - Because of time constraint, was not able to quantify the DNA concentration
- - Sitting in the freezer of Olin 301
Afternoon lab work done by: Nancy Li, Youjin Cho
- After 5 hours of subculturing, transferred all the samples into corresponding 50mL tubes and spun them down at 4500rpm for 30 minutes
- Poured off the supernatant and stored the pellets at -20°C for future use
Thursday, September 22
Afternoon lab work done by: Charlie Chung
- Quantified the Miniprep-purified products with NanoDrop
- - VioA-1 = 68ng/µL
- - VioA-2 = 60.2ng/µL
- - VioA-3 = 88.1ng/µL
- - VioB-1 = 117.6ng/µL
- - VioB-2 = 89ng/µL
- - VioB-3 = 133.6ng/µL
- - VioE-1 = 80.5ng/µL
- - VioE-2 = 73.6ng/µL
- - VioE-3 = 77.4ng/µL
- - RFP-1 = 84.4ng/µL
- - RFP-2 = 56.5ng/µL
- Prepared samples for sequencing submission
- Order Number:10257313
- VioA-1
- 15µL VioA-1+pZE12 (1µg)
- 2µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioA-2
- 17µL VioA-2+pZE12 (1µg)
- 1µL pZE12 forward primer
- 18µL Total
- VioA-3
- 12µL VioA-3+pZE12 (1µg)
- 5µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioB-1
- 9µL VioB-1+pZE12 (1µg)
- 8µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioB-2
- 12µL VioB-2+pZE12 (1µg)
- 5µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioB-3
- 9µL ddH2O
- 8µL VioB-3+pZE12 (1µg)
- 1µL pZE12 forward primer
- 18µL Total
- VioE-1
- 13µL VioE-1+pZE12 (1µg)
- 4µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioE-2
- 14µL VioE-2+pZE12 (1µg)
- 3µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- VioE-3
- 13µL VioE-3+pZE12 (1µg)
- 4µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- RFP-1
- 12µL RFP-1+pZE12 (1µg)
- 5µL ddH2O
- 1µL pZE12 forward primer
- 18µL Total
- RFP-2
- 17µL RFP-2+pZE12 (1µg)
- 1µL pZE12 forward primer
- 18µL Total
Friday, September 23
Afternoon lab work done by: Charlie Chung
- Picked two colonies each from Sean's GFP+AviTag+pZE12 and RFP+AviTag+pZE12 plates and started (3mL LB + 3µL ampicillin) cultures
- - Shaking at 37°C in Weill Hall
Saturday, September 24
Microfluidics work done by: Maneesh Gupta
- ...
Lab work done by: Jim Mathew, Nancy Li, Charlie Chung, Claire Paduano
- PCR
