Template:Team:UC Berkeley/Notebook/CDB notes

From 2008.igem.org

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(New page: June 4, 2008 - Today we continued training and discussed the project.)
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June 4, 2008 - Today we continued training and discussed the project.
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6/4/08 - Today we continued training and discussed the project.
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6/6/08 - Jin streaked a plate with MC1061 E. coli cells and incubated at 37 C.
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6/7/08 - Plate moved to fridge.
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6/8/08 - I chose an isolated colony from the plate and inoculated a few mL of fresh LB media with it. The tube was incubated on a shaker at 37 C for 24 hrs.
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6/9/08 - Took 200 uL of saturated culture and added it to 8 mL of LB media at 10:45 AM. Grew for 2 hrs on a shaker at 37 C.
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Split culture into 3 tubes with 2 mL each.
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culture 1 - Control (no sound), grew in foam box
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culture 2 - Music, high volume for 1 hr.
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culture 3 - Ultrasound bath for 1 hr.

Revision as of 17:55, 9 June 2008

6/4/08 - Today we continued training and discussed the project.

6/6/08 - Jin streaked a plate with MC1061 E. coli cells and incubated at 37 C. 6/7/08 - Plate moved to fridge. 6/8/08 - I chose an isolated colony from the plate and inoculated a few mL of fresh LB media with it. The tube was incubated on a shaker at 37 C for 24 hrs.

6/9/08 - Took 200 uL of saturated culture and added it to 8 mL of LB media at 10:45 AM. Grew for 2 hrs on a shaker at 37 C. Split culture into 3 tubes with 2 mL each. culture 1 - Control (no sound), grew in foam box culture 2 - Music, high volume for 1 hr. culture 3 - Ultrasound bath for 1 hr.