Team:KAIT Japan/Notebook

From 2012.igem.org

(Difference between revisions)
(→Colony PCR)
(→PCR Product 1,3,9)
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'''→Reflection:Band was less.'''
'''→Reflection:Band was less.'''
#Storage
#Storage
-
===PCR Product 1,3,9===
+
===PCR Production===
#Electrophoresis
#Electrophoresis
#*The gel check and cut
#*The gel check and cut

Revision as of 16:15, 13 August 2012

KAIT_Japan_Rogo2mini.png

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During the creation.
Creating parts of Tar methylation region.

Contents

Date: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:Took colony too many.You should take less colony.
Conditions of the thermal cycler

  1. 95℃(5min)
  2. 94℃(30sec)
  3. 61℃(30sec)
  4. 71℃(40sec)
  5. 72℃(1min)
  6. 4℃(Save)
    • 2~4:35cycle→Reflection:The number of cycles was less.So,We increased The number of cycles in 8/11.(50 cycles)

Date: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:30min

→Reflection:Band was less.

  1. Storage

PCR Production

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

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