Team:UCLA/Notebook/Recombinant Expression/9 July 2015
Protocol 1. Chill a 50mL Falcon tube on ice. Add 2mL of resin slurry. 2. Centrifuge the tube for 2 minutes at 700g. Remove supernatant. NOTE: The speed was increased to 1,000g and then 3,000g to maximize the amount of ethanol supernatant. 3. Add 2 bed volumes (BV) of 1X binding buffer to resin and mix thoroughly on a rotary spinner until buffer is fully suspended in resin. 4. Centrifuge tube for 2 minutes at 700g. Remove buffer. 5. Add protein lysate diluted in 1X binding buffer in 1 to 1 volume ratio to tube. Mix for 30 minutes on an end over end rotation vehicle (rotary spinner). 6. Centrifuge the tube for 2 minutes at 700g. Decant supernatant and collect as Fraction 1. 7. Wash with 2 BV's of 1X wash buffer (20 mM Imidazole). Centrifuge for 2 minutes at 700g. Decant supernatant and collect as Fraction 2. 8. Wash with 2 BV's of 1X wash buffer (50 mM Imidazole). Centrifuge for 2 minutes at 700g. Decant supernatant and collect as Fraction 3. 9. Elute using 1 BV of elution buffer (100 mM Imidazole). Centrifuge for 2 minutes at 700g. Decant supernatant and collect as Fraction4. 10. Repeat elution with 250 mM imidazole solution. Centrifuge for 2 minutes at 700g. Decant supernatant and collect as Fraction 5.