Team:UPO-Sevilla/Notebook/10 07
From 2010.igem.org
October, 7th
Assay Team
Inocula of 16+3/3T5 different colonies were set up.
Inocula of UPO4, 5 and 11/1C3 different colonies were set up.
Digestion of UPO 13+3 (2h, 37ºC) to clone them at pSB3T5 (final vector of 12+2+13+3 circuit). Digestion was run in a 0.8% agarose gel and the positive spot was isolated and purified using GFX. The purification was quantified by Nanodrop. Ligation of 13+3/3T5.
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