Team:USTC/Standard & Protocol
From 2009.igem.org
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===Colony PCR=== | ===Colony PCR=== | ||
==Measurement protocol== | ==Measurement protocol== | ||
+ | ===Promoter measurements=== | ||
+ | 1. Streak a LB plate of the strain which contain one of the parts listed in pSB1A3 . | ||
+ | |||
+ | 2. Inoculate two 3ml cultures of supplemented M9 Medium and antibiotic( Ampicillin 0.1mg/ml) with single colony from the plate. | ||
+ | |||
+ | 3. Cultures were grown in test tubes(BIO BASIC INC.12ml Polypropylene Round-bottom Culture Tubes With Graduations And Dual Cap Cat.No:TD444) for 16hrs at 37℃ with shaking at 200rpm. | ||
+ | |||
+ | 4. Cultures were diluted 1:100 into 3ml fresh medium and grown for 3hrs. | ||
+ | |||
+ | 5. Measure the fluorescence(SHIMDZU SPECTROFLUOROPHOTOMETER RF-5301PC, 250ul quartz cell path length 10mm,501 nm excitation,514 nm emission,1.5nm slit width) and absorbance (HITACHI UV-VIS spectrophotometer U-2810 ,200ul quartz cell,path length 10mm,600nm,1.5 nm slit width) every 30 minutes in the next 4hrs. |
Revision as of 17:19, 20 October 2009
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Team:USTC/Standard & Protocol
Contents |
Standard protocol
Minipreps
Performed with BIO BASIC INC. EZ-10 Spin Column Plasmid DNA MiniPreps Kit BS414
Digestion
The digestion enzymes we use are listed:
Pst I Fermentas ER0611 3000U
EcoR I Fermentas ER0271 5000U
Spe I Fermentas ER1251 1500U
Xba I Fermentas ER0681 400U
Gel Extraction
Performed with BIO BASIC INC. EZ-10 Spin Column DNA Gel Extraction Kit BS354
Ligation
For short segments:
TakaRa DNA Ligation Kit Ver2.0 Code D6022
BIO BASIC INC. FAST LIGATION KIT BS512
For long segments ligation:
TaKaRa DNA Ligation Kit LONG Code D6024
Transformation
Colony PCR
Measurement protocol
Promoter measurements
1. Streak a LB plate of the strain which contain one of the parts listed in pSB1A3 .
2. Inoculate two 3ml cultures of supplemented M9 Medium and antibiotic( Ampicillin 0.1mg/ml) with single colony from the plate.
3. Cultures were grown in test tubes(BIO BASIC INC.12ml Polypropylene Round-bottom Culture Tubes With Graduations And Dual Cap Cat.No:TD444) for 16hrs at 37℃ with shaking at 200rpm.
4. Cultures were diluted 1:100 into 3ml fresh medium and grown for 3hrs.
5. Measure the fluorescence(SHIMDZU SPECTROFLUOROPHOTOMETER RF-5301PC, 250ul quartz cell path length 10mm,501 nm excitation,514 nm emission,1.5nm slit width) and absorbance (HITACHI UV-VIS spectrophotometer U-2810 ,200ul quartz cell,path length 10mm,600nm,1.5 nm slit width) every 30 minutes in the next 4hrs.