Bacterial Transformation for Bio113

Transforming DNA after GGA Ligation

1. Thaw the competent cells on ice for 6 minutes. Each tube contains 50 µL of E. coli, JM109 cells.
2. 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.
3. Incubate on ice for 5 minutes.
4. Add 30 µL SOC media with no antibiotic to your transformed cells. Spread cells onto LB plates containing ampicillin.

You're done already!!