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Team:HokkaidoU Japan/Notebook/plastic Week 11
From 2012.igem.org
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| - | + | RBS-PhaB was ligated with dT on pSB1AK3.<br/> | |
| + | We added LB to fungus liquid mixed ligated DNAs and then spread it on LBK plates. | ||
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Revision as of 03:12, 13 September 2012
Contents |
September 10th
PCR
PhaA was multiplied from pGEM with XbaI and SpeI restriction sites by PCR.
Digestion
PhaA was digested with XbaI and SpeI. RBS on pSB1A2 was digested with SpeI.
Gel extraction
We confirmed succession of digestion by electrophoresis.
And then DNA were extracted from TBE gel.
Ligation
RBS on pSB1A2 was ligated with PhaA and PhaB.
Transformation
These ligated DNAs transformed into E.coli (strain: DH5α).
And then we spread fungus liquid added LB on plates.
September 11th
sequence
We analyzed the sequence which contains phaA to see if there is a mutation.
Colony PCR
The colony of RBS+phaB on 1A2 was
September 13th
Digestion
We were worried about yesterday lab work, so tried it again.
RBS-PhaB on pSB1A2 was digested with EcoRI and SpeI restriction sites and dT(B0015) on pSB1AK3 was also digested with EcoRI and XbaI.
Gel extraction
We confirmed the succession of digestion by electrophoresis.
And extracted the DNAs from TBE gel.
Ethanol precipitation
The DNA solution of RBS-PhaB and dT on pSB1AK3 were concentrated by EtOH precipitation.
Ligation
RBS-PhaB was ligated with dT on pSB1AK3.
We added LB to fungus liquid mixed ligated DNAs and then spread it on LBK plates.
