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Team:Warsaw/Calendar-Stage1/19 August 2010
From 2010.igem.org
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.
(zdjęcie)
