產(chǎn)品名稱：5XRIPABufferwithProteaseInhibitorCocktail

• Buffer is able to extract cytoplasmic, membrane, and nuclear proteins
• Suitable for downstream assays such as reporter assays, protein assays, immunoassays and protein purification
• Protease Inhibitor Cocktail included

1X RIPA Buffer: Mix the 5X RIPA Buffer by inverting/vortexing the bottle a few minutes. Dilute the 5X RIPA Buffer to 1X with deionized water. Stir to homogeneity. Store at 4?°C for up to 6 months. Protease Inhibitor Cocktail: Immediately before use dilute the Protease Inhibitor Cocktail 1:100 with 1X RIPA Buffer. Stir to homogeneity. Do not store diluted solutions containing protease inhibitors.

I. Adherent Cells

1. Culture cells to approximately 80-90?% confluence.
2. Aspirate the culture media and wash twice with cold PBS.
3. Add cold 1X RIPA Buffer to the cells, spreading evenly. Use 1?mL of buffer per 10-cm dish 2 (56.7 cm ), maintaining on ice for 5?minutes. Cells may be scraped with a cell scraper.
4. Collect the lysate into a microcentrifuge tube.
5. Centrifuge for 10?minutes (14000 x g).
6. Transfer the supernatant to a clean tube and maintain at 4?°C. Samples may be frozen at -80?°C.

II. Suspension Cells

1. Collect the cells into an appropriate conical centrifuge tube.
2. Centrifuge for 5?minutes (600 x g).
3. Remove and discard the supernatant.
4. Wash the cells twice with cold PBS, centrifuging for 5?minutes between (600 x g).
5. Add cold 1X RIPA Buffer to the cell pellet. Use 1?mL of buffer per 40?mg of wet cell pellet. Gently resuspend the pellet by pipetting up and down.
6. Shake the suspension for 15?minutes at 4?°C.
7. Centrifuge for 10?minutes (14000 x g).
8. Transfer the supernatant to a clean tube and maintain at 4?°C. Samples may be frozen at -80?°C.