Template:Team:Groningen/CONTENT/EXPERIMENTS/tasA Heat Shock Transformation in E. coli (t16)

00:00, 21 May 2015 - 00:00, 21 May 2015
The mixture was incubated at room temperature for 2 hours. During this time ampicillin plates were poured (100 µg/mL). Afterwards the heat shock transformation was carried out using the following components.
10 µL ligation mixture in competent DH5 alpha
Competent cells Harm (E.coli (1)) (CompH)
Competent cells Clement (CompC)
The transformed cells were plated on LB+amp plates.
90% CompH
10% CompH
90% CompC
10% CompC
The plates were put in the incubator overnight at 37 °C.
Harm Ruesink
00:00, 22 May 2015 - 00:00, 22 May 2015
The transformation was checked. There were 5 colonies visible on the LB+amp plates. 4 colonies on 90% compH and one colony on 10% CompH. Both plates were stored in the fridge at 4 °C.
Harm Ruesink


00:00, 26 May 2015 - 00:00, 26 May 2015
The five transformed colonies were inoculated overnight in liquid LB+amp (30 µL amp per 3 mL LB (1/100)). This should have been 3 µL per 3 mL amp, so also this concentration was made and used. The culture of the colony from the 10% plate was labeled sample 1 and the cultures of the four colonies from the 90% plate were labeled sample 2, 3, 4 and 5. The cultures were incubated at 37 °C, at 250 rpm.
Harm Ruesink