Team:Northwestern/Protocol
From 2010.igem.org
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===[[LIVE/DEAD® BacLight - Bacterial Viability Kit]]=== | ===[[LIVE/DEAD® BacLight - Bacterial Viability Kit]]=== |
Revision as of 19:28, 14 August 2010
Home | Brainstorm | Team | Acknowledgements | Project | Side Project | Parts | Notebook | Calendar | Protocol | Safety | Links | References | Media | Contact |
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Contents |
DNA
Prepping DNA from the kit plates
Quikchange (from primers to colonies!)
Kit to Stock Plasmid
Ethanol Precipitation
New Part Design(PCR)
Bacterial Work
Transformation
O/N Culture
Preparation of Competent Cells
LB Media
Preparing Plates
Glycerol Stocks
Assembly
Restriction Enzyme Digests
Plasmid Construction
3A Assembly
Ligations
Mini Prep
Microscopy
Confocal Microscopy
Fluorescence Microscopy
Reagents
Reagents
Cell Staining
Rhodamine-Conjugated Chitin Probe
Methanol Fixation
- Rinse slide with ethanol and flame
- Rinse slide with PBS and dry with KimWipe
- Apply cell sample to microscope slide and let air dry
- Submerge in -20C absolute methanol for 5-10 min
- Wash 3 times with 1X TBS (submerge in 1X TBS for 5 minutes per wash)
- Do not let cells dry for the rest of the procedure