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Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/26
From 2010.igem.org
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Revision as of 05:42, 8 September 2010
Contents |
PCR
member
same above
Materials
- 2×PCR buffer 25×4μl
- 2mM dNTP 10×4μl
- 10mM primer(sense)bcsA,B,C and D 2.5μl each
- 10mM primer(antisense)bcsA,B,C and D 2.5μl each
- template DNA a little
- Q water 9×4μl
- KOD FX 0.5×4μl
Procedure
①mix all materials for 4 tubes.
②elongation
- bcsA,bcsB and bcsC
- 94℃ 2min
- 98℃ 10sec☆
- 55℃ 30sec
- 68℃ 4min★
- 68℃ 7min
- 10℃ ∞
- bcsD
- 94℃ 2min
- 98℃ 10sec☆
- 55℃ 30sec
- 68℃ 1min★
- 68℃ 7min
- 10℃ ∞
※30cycle ☆ to ★.
