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Template:Team:UC Berkeley/Notebook/BX notes
From 2008.igem.org
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Sixpi 23:31, 9 June 2008 (UTC)
Today I poured plates. There were 3 liters of LB/agar media, to which I added Spectinomysin.
Sixpi 00:02, 5 June 2008 (UTC)
In our demos this morning we transformed bacteria, plated them, picked colonies, grew them up, and extracted DNA. The afternoon was taken up by designing oligos for the basic parts will start making next week(hopefully).
Sixpi 05:12, 4 June 2008 (UTC)
Today we continued our part making demo. Yesterday we set up the PCR reaction, and today we cleaned up the PCR, set up the digestion, and also ran an analytical gel of the PCR product.
