Team:Tokyo Metropolitan/Notebook/Pattern/2010/08/28

From 2010.igem.org

Revision as of 08:46, 4 September 2010 by Hitomi (Talk | contribs)


Contents

2010/08/28

1:PCR

<Member>
Mariko, Hitomi


<Sample>
・E-coli (having BBa_I732901 plasmid)


<Protocol>
See Protocol 2

・Tube(higher temperature/lower temperature in annealing)

  1. Rfp (67.5℃/66.0)
  2. Terminator (66.0/63.0)

Total 4 tubes.


2:Plasmid extraction from E-coli

<Member>
Hitomi


<Sample>
・transformed E-coli (8/26)

  • BBa_I13521
  • BBa_B0010
  • BBa_B0030
  • BBa_J23110
  • BBa_E0040


<Protocol>
SeeProtocol 6


3:DNA concentration measurement

<Member>
Hitomi


<Sample>
・PCR products


<Protocol>

  1. Add 2µl of TE and 2µl of sample into the tube, and mix it gently.
  2. Fall in drops 1 on the measuring machine.


<Result>

DNA concentration
concentration A320 A260/A280 A260/A230
RH 565.0 20.24 1.723 1.175
RL 400.5 10.73 1.697 1.462
TH 356.0 8.47 1.622 1.201
TL 324.5 8.31 1.627 1.195


4:Electrophoresis

<Member>
Mariko, Hitomi


<Sample>
・PCR products


<Protocol>
SeeProtocol 8


<Result>