Uppsala-Sweden/17 September 2009
From 2009.igem.org
Colony PCR of yesterdays transformations
The colony PCR was this time performed utilizing dream taq.
Weseem to have good transformations of R-Kivd (2, 5), KRYT (4, 5, 6). Quite a meager turnout of that many transformations, something still screws up the process.
Pictures:
inoculate RKivd, 2 5, KRYT 4, 5, 6 only. --Anders 15:11, 21 September 2009 (UTC)
Evaluation of EcorI, SpeI and Adh2Z
Due to poor transformation efficiency we decided to evaluate the restriction enzymes by single and double digestion of RPRAT
The result:
The triple bands from the RPRA EcorI digestion can be explained by additional restriction by that enzyme forming Single and double restriction products. ~6kb plasmid + RPRAT, ~3.3 kb plasmid + RPRAT fragment, ~2.7 kb RPRAT fragment.
We conclude fault in EcorI or RPRAT.
--Anders 20:56, 19 October 2009 (UTC)