Team:UNIPV-Pavia/Protocols/Transformation
From 2008.igem.org
Home | The Team | The Project | Biological Safety | Parts Submitted to the Registry |
---|---|---|---|---|
Dry Lab | Wet Lab | Modeling | Protocols | Activity Notebook |
Transformation
(estimated time: 3 hours and 30 min + 12-14 hours overnight incubation)
Materials needed:
- LB agar plates with proper antibiotic added incubated at 37°C
- Thawed Invitrogen TOP10 cells (every tube contains approximately 60 )
- Resuspended DNA
- SOC medium
- Cut paper spots using scalpel and tweezers (or punch tool, following provided instructions); if you use scalpel and tweezers, try to cut pieces of about the same dimension of the punch tool.
- Clean scalpel and tweezers (or punch tool) with water and ethanol every time you cut a spot; be careful to dry your tools correctly, especially if you use punch tool, which needs more time to dry than scalpel/tweezers.
- Put the cut paper into the 0.5 ml tube.
- Incubate at 42°C for 20 min.
- Vortex and spin down.