Abcam's 10X RIPA lysis buffer is an efficient means of cell lysis and protein solubilization for both adherent and suspension cultured mammalian cells.
IP, ELISA, SDS-PAGE, WB
Liquid
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application IP | Reactivity Reacts | Dilution info - | Notes Suggested working concentration: 1X |
Application ELISA | Reactivity Reacts | Dilution info - | Notes Suggested working concentration: 1X |
Application SDS-PAGE | Reactivity Reacts | Dilution info - | Notes Suggested working concentration: 1X |
Application WB | Reactivity Reacts | Dilution info - | Notes Suggested working concentration: 1X |
Abcam's 10X RIPA lysis buffer is an efficient means of cell lysis and protein solubilization for both adherent and suspension cultured mammalian cells.
IP, ELISA, SDS-PAGE, WB
Liquid
pH: 7.5
Constituents: 10% Nonylphenol, ethoxylated, 8.8% Sodium chloride, 6.1% Tris, 5% Sodium deoxycholate, 1.12% Sodium pyrophosphate decahydrate, 1% Sodium lauryl sulfate, 0.38% EGTA, 0.29% EDTA, 0.22% Beta glycerophosphate, 0.18% Sodium orthovanadate
Ambient - Can Ship with Ice
Ambient
Ambient
Abcam's 10X RIPA lysis buffer is an efficient means of cell lysis and protein solubilization for both adherent and suspension cultured mammalian cells. This reagent effectively extracts cytoplasmic, nuclear and membrane proteins. It is compatible with many downstream applications, including SDS-PAGE, Western blot, immunoprecipitation, ELISA and BCA assays.
Preparation: Dilute to 1X in deionized water
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HeLa cell extraction using ab156034.
2.5 million HeLa cells were lysed on ice for 15 minutes with 0.5 mL of 1X ab156034. Next the sample was centrifuged at 14,000 rpm at 4ºC for 15 minutes: the supernatant ( = cleared lysate) was removed and the pellet ( = insoluble material) was resuspended in 0.5 mL lysis buffer and solubilized by sonication. Equivalent loads of the cleared lysate and solubilized pellet were analyzed by SDS-PAGE and Coomassie stain.
BCA protein concentration determination of the soluble and insoluble material indicates that a total of 1.1mg of protein was recovered and 82% was in the soluble cleared cell lysate.
Lane 1: MW marker
Lane 2: Cleared lysate
Lane 3: Non-soluble
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