IGEM:MIT/2006/Notebook/2007-6-19
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Things to do Today
1. Take the culture from last night out- DONE
2. Take OD600s of the culture- DONE (all 2.00)
3. Spike culture with methyl salicylate- DONE (.1 ppm, 1 ppm, 5 ppm, 10 ppm, 25 ppm, and negative control)
4. Extract samples from the culture- DONE
5. Repeat to 1) for next culture- DONE FOR ALL
6. Set up reservation for GC/MS- DONE (3:00)
7. Do GC/MS for samples- WORKING ON IT
8. Edit introduction from yesterday- DONE (to some degree)
9. Check sequencing results- some look good (will look with Barry to confirm
10. Make two 25 mL cultures (J45120 + salicylic acid and J45200 + isoamyl alcohol) for Drew- DONE