IGEM:MIT/2006/Notebook/2007-1-31

Plan

1. Make reservations for the plate reader- DONE

2. Make reservations for the GC (isoamyl acetate samples)- DONE

3. Dilute the osmY and control cultures and grow them up for 3 hours before running on the plate reader- DONE

4. Run the osmY and control cultures on the plate reader

5. Submit the plates streaked out last night to the Registry- NOT DONE (tried to submit to Knight lab today but nobody was there; will give them to someone from the Knight lab at the 4 PM meeting)

6. Finish extracting the isoamyl acetate cultures- DONE

7. Run the isoamyl acetate cultures on the GC- DONE

8. Update google doc for the meeting- DONE

9. Get organized for the meeting at 4 PM- DONE

10. Move initial plate reader results to the wiki for the meeting- DONE

11. Go to the meeting at 4 PM on the status of the research

12. Analyze GC results