From 2013.igem.org
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| #Storage | | #Storage |
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| + | =='''Colony PCR'''== |
| + | :'''Reagent''' |
| + | :*TaKaRa Ex Taq(5units/μL) 0.5μL |
| + | :*10×Ex Taq buffer 10μL |
| + | :*dNTP Mixture(2.5Meach) 8μL |
| + | :*Primer F(10μM) 4μL |
| + | :*Primer R(10μM) 4μL |
| + | :*Template(E.coli DH5α) |
| + | :*sterilized water(73.5μL) |
| + | :'''Conditions of the thermal cycler''' |
| + | #95°C(2min) |
| + | #95°C(30sec) |
| + | #54°C(30sec) |
| + | #72°C(40sec) |
| + | #72°C(5min) |
| + | #4°C(Save) |
| + | #*2-4:40cycle |
| + | #*gradient:57-62°C(+0.1c) |
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Revision as of 04:09, 19 August 2013
- Home
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- Parts
Protocol
- Notebook
- Results
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- Human Practice
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Protocol
Miniprep
- Add culture medium 1mL in a microtube
- Centrifuge(1min,4°C,10,000rpm)
- Remove the supernatant to new microtube
- Repeat 1-3
- Add SolI 100μL and Vortex
- Add SolII 200μL and invert
- ice-cold 3min
- Add SolIII 150μL and invert
- ice-cold 3min
- Centrifuge(10min,4°C,10,000rpm)
- Add the supernatant to new microtube
- Add RNase 0.8μL
- Incubation(1h,37°C)
- Add phenol:chloroform 200μL
- Vortex
- Centrifuge(5min,4°C,10,000rpm)
- Add the supernatant to new microtube
- Add chloroform 200μL
- Tapping
- Centrifuge(1min,4°C,10,000rpm)
- Add the supernatant(150μL) to new microtube
- Add 3M-acetic acid 15μL
- Add 100%Et 400μL and invert
- Centrifuge(20min,4°C,10,000rpm)
- Remove the supernatant to new microtube
- Add 70%Et 400 μL
- Tapping
- Centrifuge(20min,4°C,10,000rpm)
- Remove the supernatant to new microtube
- Dry
- Add TE buffer 50μL
- Storage
Colony PCR
- Reagent
- TaKaRa Ex Taq(5units/μL) 0.5μL
- 10×Ex Taq buffer 10μL
- dNTP Mixture(2.5Meach) 8μL
- Primer F(10μM) 4μL
- Primer R(10μM) 4μL
- Template(E.coli DH5α)
- sterilized water(73.5μL)
- Conditions of the thermal cycler
- 95°C(2min)
- 95°C(30sec)
- 54°C(30sec)
- 72°C(40sec)
- 72°C(5min)
- 4°C(Save)
- 2-4:40cycle
- gradient:57-62°C(+0.1c)
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