Team:Warsaw/Calendar-Stage1/19 August 2010


Revision as of 13:13, 31 July 2010 by KasiaG (Talk | contribs)

Example Tabs

Cloning Fluorescent proteins behind J23100 (without RBS) - continuation [Ania P.]

Repeating of transformations from friday 16 July (because there was nothing on the plates).

Cloning mCherry NLS behind Anderson's RBS (Ba_J61101) [Ania P., Milena, Kasia]

1. Digest of mCherry NLS with XbaI/PstI for 3 hours.
2. Electrophoresis (whole sample put on the gel).
There was not enough DNA to cut it out and isolate from agarose gel.