Team:Tokyo Metropolitan/Notebook/Pattern/2010/08/30

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=2010/08/30=
=2010/08/30=

Latest revision as of 18:12, 24 October 2010


E.coli Pattern Formation Project Notebook



August 2010
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September 2010
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Contents

2010/08/30

1:PCR

<Member>
Mariko, Hitomi, Taka


<Sample>
・E-coli (having BBa_I13521 plasmid)

・E-coli (having BBa_K208017 plasmid)

・E-coli JM109 (NIPPON GENE)


<Protocol>
See Protocol 2

・Tube (temperature in annealing)
1.Promoter~signal (72.0℃)
3. mRFP~Terminator (69.0)
4. Promoter (70.0)
5. RBS~signal (70.0)
7. Terminator (69.0/67.5/66.0)
8. CRP (72.5)

Total 8 tubes.


2:DNA Digestion

<Member>
nito


<Sample, Materials>
・PCR productions

  • 1L(8/25) 8μl
  • 2L(8/26) 8μl
  • 4H(8/26) 16μl
  • 5H(8/26) 16μl

・Digest enzyme

  • AvrⅡ
  • NheⅠ
  • SpeⅠ


<Protocol>
See Protocol 9

3:Electrophoresis

<Member>
Mariko, Taka


<Sample>
・PCR products


<Protocol>
SeeProtocol 8


<Result>
Matsuura 2010-08-06 20hr 02min (7).JPG

4:Electrophoresis

<Member>
nito


<Sample>

(after digestion)


<Protocol>
SeeProtocol 8

And cut off gels included DNA.

<Result>
Matsuura 2010-08-06 20hr 02min (8).JPG

5:DNA Ligation

<Member>
nito


<Sample>

(after digestion)


<Protocol>
See Protocol 3

We ligated 1 and 2, 4 and 5.

6:Electrophoresis

<Member>
nito


<Sample>

(after ligation)


<Protocol>
SeeProtocol 8


<Result>
Matsuura 2010-08-06 20hr 02min (9).JPG