Team:HokkaidoU Japan/Notebook/plastic Week 13

From 2012.igem.org

(Difference between revisions)
(September 25th)
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<div class="hokkaidou-section">
<div class="hokkaidou-section">
We got colonies on the plate, and started liquid culture.
We got colonies on the plate, and started liquid culture.
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==PCR==
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<p>
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Did PCR for promoter of R.eutropha from pGEM to ligate with RBS-PhaC-RBS-PhaA-RBS-PhaB-dT on pSB1A2.
 +
</p>
 +
 +
==Digestion==
 +
<p>
 +
Digested the promoter done PCR and RBS-PhaA on pSB1A2 with XbaI and SpeI, and plasmid of RBS-PhaC-RBS-PhaA-RBS-PhaB-dT on pSB1A2 with XbaI.
 +
</p>
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 +
==Ligation==
 +
<p>
 +
Ligated the promoter with RBS-PhaC-RBS-PhaA-RBS-PhaB-dT and with pSB1A2.
 +
</p>
 +
 +
==Transformation==
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<p>
 +
Transformed each ligation product into JMi09, and incubated.
 +
</p>
</div></div>
</div></div>
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Revision as of 21:58, 26 September 2012

Contents

September 24th

Single Colony isolation

We got few colonies from the plate. The colonies were isolated to another plate.

September 25th

We got colonies on the plate, and started liquid culture.

PCR

Did PCR for promoter of R.eutropha from pGEM to ligate with RBS-PhaC-RBS-PhaA-RBS-PhaB-dT on pSB1A2.

Digestion

Digested the promoter done PCR and RBS-PhaA on pSB1A2 with XbaI and SpeI, and plasmid of RBS-PhaC-RBS-PhaA-RBS-PhaB-dT on pSB1A2 with XbaI.

Ligation

Ligated the promoter with RBS-PhaC-RBS-PhaA-RBS-PhaB-dT and with pSB1A2.

Transformation

Transformed each ligation product into JMi09, and incubated.