Bacterial Transformation for Bio113
Transforming DNA after GGA Ligation
- Thaw the competent cells on ice for 6 minutes. Each tube contains 50 µL of E. coli, JM109 cells.
- Add all 50 µL of your E. coli cells to the GGA ligation mixture. Very gently mix the DNA and cells and return the cells to ice ASAP.
- Incubate on ice for 5 minutes.
- Add 30 µL SOC media with no antibiotic to your transformed cells. Spread cells onto LB plates containing ampicillin.
You're done already!!