IGEM:MIT/2007/Notebook/2007-7-23: Difference between revisions
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#Add cells to appropriate well | #Add cells to appropriate well | ||
#Place on rocker for 1 hour at speed 5 | #Place on rocker for 1 hour at speed 5 | ||
#Aspirate out media in wells | #Aspirate/Pipet out media in wells |
Revision as of 09:30, 23 July 2007
Agenda
- Polystyrene Assay
- Morning: get correct OD
- Add AHL
- Afternoon: Test
- Digest I13500
- Ligate 3A with I13500 and Mer in pSB1AT3 (so that, if we combine with polystyrene-binding plasmid into a single cell, can test for presence of both plasmids)
- run overnight
- dilute sequencing primers
- sequence PHIE6P
- sequence F2620+B0034+CPX
- Order T7 antibody
Digestion of I13500
- Made two mixtures
4.5µl I13500(Miniprep #1, 223.5ng/µl) 1µl XbaI 1µl PstI 0.5µl BSA 5µl NEB3 Buffer 38µl H20 ------------------------- 50µl Total
- Placed in 37C @ 10:20am --> Take out @ 1:20pm
Diluted BioBrick Sequencing Primers
You can find the stock eppendorfs in the unnamed -20C fridge (Jason+Barry's room).
Diluted from 100µM stock to 32.2µM with total volume of 1.55mL each.
Made 1 VF2 and 1 VR for iGEM use.
Polystyrene Assay Protocol
- Cell Lines:
- Controls: DH5-alpha (not transformed)
- FHUA PHIE6 --> IPTG
- CPX --> AHL
- Media:
- H20
- PBS
- PBS + Tween + BSA
- Protocol
- Add AHL/IPTG to Liquid Culture
- Wait an hour for AHL induced expression
- Incubate wells in wash media for 30 minutes on rocker at speed 5
- Centrifuge cells out of Liquid Culture media
- Resuspend in wash media
- Add cells to appropriate well
- Place on rocker for 1 hour at speed 5
- Aspirate/Pipet out media in wells