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6 h later cells were collected, and directly lysed using RIPA buffer (150 mM NaCl, 50 mM Tris-HCl [pH 8.0], 5 mM EDTA pH 8.0, 0.5% NP-40, 0.5% Triton X-100, 0.5% sodium deoxycholate, 0.1% SDS, 1 cOmplete Mini protease inhibitor cocktail (Roche), 1 PhosSTOP phosphatase inhibitor cocktail (Roche), 10 M MG132)

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The choice among these approaches depends entirely on the specific research question, the preferred administration route, and the research timeline being studied

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476 : 5254 Barford D (2004) The role of cysteine residues as redox-sensitive regulatory switches
