Team:Tokyo Metropolitan/Notebook/Fiber/2010/10/06

From 2010.igem.org

(Difference between revisions)
(New page: ==2010/10/06 Wednesday (Naoto)== ===Experiment:Electrophoresis of insert check PCR=== '''member''' naoto '''material''' *insert check PCR production(PCR at 10/05) If you want to know o...)
Line 1: Line 1:
 +
{{:Team:Tokyo_Metropolitan/Header}}
 +
==2010/10/06 Wednesday (Naoto)==
==2010/10/06 Wednesday (Naoto)==
===Experiment:Electrophoresis of insert check PCR===
===Experiment:Electrophoresis of insert check PCR===

Revision as of 02:53, 11 October 2010


Contents

2010/10/06 Wednesday (Naoto)

Experiment:Electrophoresis of insert check PCR

member

naoto

material

  • insert check PCR production(PCR at 10/05)

If you want to know other materials,see protocol4

procedure

see protocol4

result

All of bands seemed to be vector self ligation

Experiment:PCR of T7promoter~bcsABCD(A.xylinum),T7promoter~bcsEFG(E.coli),RBS~T7polymerase

member

naoto

material

  • A colony of A.xylinum
  • bcsEFG(E.coli)
  • T7 polymerase(BBa_K145001)

If you want to know other materials,see protocol3

procedure

see protocol3

Experiment:Measure DNA density

member

naoto

material

  • absorption spectrometer
  • bcsA,B,C,D(A.xylinum)
  • bcsA,B,C,EFG(E.coli)
  • pSB1C3
  • TE buffer

procedure

  • mix 2µl of DNA solution with 2µl of TE buffer
  • spot DNA solution and TE buffer mixture to absorption spectrometer
  • measure DNA density