IGEM:MIT/2006/Notebook/2006-6-20

To do

1. Set up and run gradient PCR for BAMT and SAMT
2. run test gels on exhaustive BAMT and SAMT pcr products - possibly reconsider primers
3. Reconsider ATF1 primers definitely
4. Grow colonies on sketchy minimal media plates
5. Smell LB liquid and minimal liquid cultures
6. Pour new minimal plates
7. Get in touch with GC lab