Team:KAIT Japan/Notebook

From 2012.igem.org

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*Primer R(10μM) 4μL
*Primer R(10μM) 4μL
*Template(E.coli DH5α)
*Template(E.coli DH5α)
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**'''Reflection:'''
+
**'''Reflection:You should take less colony.'''
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==8/11==
==8/11==

Revision as of 02:38, 13 August 2012

KAIT_Japan_Rogo2mini.png

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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:You should take less colony.

8/11

The purified DNA1,2

  1. Electrophoresis
    • Marker:pigment(buffer) 1μL,DNA molecule 2μL,TE buffer 3μL
    • Sample:pigment(buffer) 1μL,sample 5μL
    • Gel concentration:1.2%,Migration time:30minutes
  2. Storage

PCR Product 1,3,9

  1. Electrophoresis
    • The gel check and cut
  2. DNA purification
  3. Confirmation of electrophoresis
  4. PCR
    • 50cycle
  5. Storage