From IGEM07

Transformation of plasmid DNA to competent E. Coli cells

Material and Reagents

        1. SOC

           2% Tryptone
           0.5% Yeast Extract
           10mM NaCl
           10mM MgSO4
           10mM MgCl2
        2. 1.5 mL microfuge tubes
        3. 42° C waterbath
        4. Ice
        5. 37° C shaker

Protocol

        1. Thaw competent cells on ice. 20–200µL per tube
        2. Add max. 20µL of a ligation reaction
        3. Mix very gently!
        4. Incubate the tubes on ice for 30 min
        5. Heat shock the cells for 30 sec at 42°C
        6. Place the tubes immediately on ice for at least 2 min
        7. Add 250µL of SOC medium to each tube
        8. Incubate for 1 hour at 37°C and shake vigorously
        9. Plate out the suspension on a LB agar plate containing the appropriate antibiotic.
       10. Incubate the plates overnight at 37°C