Team:HokkaidoU Japan/Notebook/September7
From 2010.igem.org
(Difference between revisions)
(→エタ沈) |
(→コンピテントセルのPCR) |
||
Line 9: | Line 9: | ||
In acordace to Mighty Mix default protocol that for ligation DNA must melted in TE and for concentrating it more Ethanol percipication was done. | In acordace to Mighty Mix default protocol that for ligation DNA must melted in TE and for concentrating it more Ethanol percipication was done. | ||
- | == | + | ==Colony PCR of competent cells== |
- | + | ||
- | * | + | Previous colony PCR produced strange bands so checked if there were from DNA of competent cell |
+ | * Colony PCR didn`t produce any bands so those bands had to be an artifact from plasmid used for transformation |
Revision as of 17:53, 27 September 2010
Checked concentration of DNA used yestrday for ligation
- 4 ng/uL RFP digested using either H buffer and M buffer
- pSB1C3 band was very week
Ethanol percipication
In acordace to Mighty Mix default protocol that for ligation DNA must melted in TE and for concentrating it more Ethanol percipication was done.
Colony PCR of competent cells
Previous colony PCR produced strange bands so checked if there were from DNA of competent cell
- Colony PCR didn`t produce any bands so those bands had to be an artifact from plasmid used for transformation