Team:KAIT Japan/Notebook
From 2012.igem.org
(Difference between revisions)
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==8/9== | ==8/9== | ||
- | + | ===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) | ||
+ | **'''Reflection:''' | ||
+ | ---- | ||
==8/11== | ==8/11== | ||
===The purified DNA1,2=== | ===The purified DNA1,2=== |
Revision as of 02:37, 13 August 2012
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During the creation
Contents |
8/9
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)
- Reflection:
8/11
The purified DNA1,2
- Electrophoresis
- Marker:pigment(buffer) 1μL,DNA molecule 2μL,TE buffer 3μL
- Sample:pigment(buffer) 1μL,sample 5μL
- Gel concentration:1.2%,Migration time:30minutes
- Storage
PCR Product 1,3,9
- Electrophoresis
- The gel check and cut
- DNA purification
- Confirmation of electrophoresis
- PCR
- 50cycle
- Storage