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Control Cell Lysates
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Description:
Control cell lysates from Raji cells, human B lymphocytes from Burkitt's Lymphoma, were cultured in the presence of media containing 10% FCS. Cells were lysed in RIPA buffer (50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1 mM EDTA, 1 mM NaF, 1 mM Na3O4, 1 mM PMSF, 1 μg/ml aprotinin, 1 μg/ml leupeptin, 1 μg/ml pepstatin, 1% NP-40, 0.25% sodium deoxycholate). 200 μg of cellular protein was mixed with the same volume of 2 X SDS-PAGE loading buffer.
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Reconstitution and Storage:
Lyophilized. Add 100 μl distilled H2O to the sample. Final concentration is 2 mg/ml. Final buffer is 31 mM Tris-HCl, pH 6.8, 5% glycerol, 1% SDS, 0.002% bromophenol blue. For long term storage store at -20°C. Avoid freeze thaw cycles.
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Key_Reference:
Ohsugi, Y., et al. (1980) J. Natl. Canc. Inst. 65:715-718; Epstein, M.A., and Barr, Y.M. (1965) J. Natl. Canc. Inst. 34:231
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Quality_Control:
35 μg of protein was loaded onto a Bio-Rad mini gel system and analyzed using 10% SDS-PAGE. Anti-Human Dbpa (Cat. No. P100916) (1:1000) was used for signal detection using an ECL-based immunoblot.
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| Suggested starting concentrations are provided.
Optimal dilutions should be determined by end-user. Differences in calculated versus apparent
molecular weight may be due to post-translational modifications or protein hydrophobicity. For
research use only not for diagnostic, human, or veterinary use. |
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Quality Control Data
35 μg of protein was loaded onto a Bio-Rad mini gel system and analyzed using 10% SDS-PAGE. Anti-Human Dbpa (Cat. No. P100916) (1:1000) was used for signal detection using an ECL-based immunoblot.
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