IGEM:MIT/2006/Notebook/2006-6-20
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To do
- Set up and run gradient PCR for BAMT and SAMT
- run test gels on exhaustive BAMT and SAMT pcr products - possibly reconsider primers
- Reconsider ATF1 primers definitely
- Grow colonies on sketchy minimal media plates
- Smell LB liquid and minimal liquid cultures
- Pour new minimal plates
- Get in touch with GC lab
- 3 pm: Stephen has meeting --- light sensor part!
WINTERGREEN!!!!!!!
- The liquid cultures from yesterday SMELLED LIKE WINTERGREEN!! SO EXCITING!!!! YAY!
- The SAMT+SA and the BSMT+SA worked, in both LB and minimal media
- Now it's time to optimize SA concentration :)
- Plated liquid cultures onto M9 with 50, 100, 200 μL SA
- 2 sets of 4 (BSMT M9, BSMT LB, SAMT M9, SAMT LB) with one set of 3 missing BSMT M9