Team:The University of Alberta/26 October 2008
From 2008.igem.org
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- | + | yesterday's transformations didn't work. not at all. no colonies. what is up with that? |
Revision as of 02:53, 29 October 2008
Jason
I performed a mini-prep of pUC57-ER, subsequently digesting it with XbaI and PstI, gel purifying the fragment and using it one of the following ligations.
I set up ligations for of pSB103+ER, pSB103+laqIQ-ERE-TetR-pTET-RFP, pSB103+pTET-BisdA-pTET-BisdB, pUC57-laqIQ-ERE-TetR-pTET-RFP+pTET-BisdA-pTET-BisdB and left them overnight at 16 degrees C.
i was awesome today.
David
yesterday's transformations didn't work. not at all. no colonies. what is up with that?