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    HeLa Whole Cell Lysate Doxorubicin Stimulated

    HeLa Whole Cell Lysate Doxorubicin Stimulated

    Catalog Number: orb348681

    DispatchUsually dispatched within 5-10 working days
    $ 394.00
    Catalog Numberorb348681
    CategoryTools
    DescriptionHeLa Whole Cell Lysate Doxorubicin Stimulated
    Tested applicationsSDS-PAGE, WB
    Concentration1.0 mg/ml
    Dilution rangeWB: User Optimized
    Form/AppearanceLiquid (sterile filtered)
    PurityThe cells were grown in DMEM supplemented with 10% FBS (Fetal Bovine Serum). Cells were treated with 0.5 µg/ml Doxorubicin for 2 h. Cells were washed in PBS and incubated on ice in modified RIPA buffer containing 150 mM sodium chloride, 50 mM Tris Cl, pH 7.4, 1 mM EDTA, 1.0% NP-40, 0.5% sodium deoxycholic acid and 0.1% SDS to lyse the cells. Protein integrity is ensured using a cocktail of protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine proteases as well as aminopeptidases (0.1 mM AEBSF HCl, 0.08 µM Aprotinin, 5 µM Bestatin, 1.5 µM E-64, 2 µM Leupeptin Hemisulfate and 1 µM Pepstatin A). Phosphatase inhibitors sodium fluoride, sodium orthovanadate, sodium pyrophosphate and -glycerophosphate were also added. Cell debris was removed by centrifugation. Protein concentration was determined by Lowry assay using a commercially available kit. The protein concentration was adjusted to 2 mg/ml and then an equal volume of 2X SDS-PAGE sample buffer was added.
    ConjugationUnconjugated
    Hazard InformationNon-Toxic
    SourceHuman
    StorageStore vial at -70° C or COLDER. For extended storage, aliquot contents to minimize freeze/thaw cycles.
    Buffer/PreservativesPreservative: None. Stabilizer: 10% (v/v) Glycerol. 1X SDS-PAGE Sample Buffer (62.5 mM Tris HCl, 2% SDS, 10% Glycerol and 0.005% bromophenol blue, pH 6.8)
    Alternative namesHeLa Whole Cell Lysate Doxorubicin Stimulated, HeL
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    NoteFor research use only
    Application notesready-to-use lysates are especially prepared as positive controls for separation by SDS-PAGE and subsequent western blot analysis. Lysates are prepared in denaturing buffer WITHOUT dissociating agents (i.e. no 2-mercaptoethanol or dithiothreitol has been added). Heat lysate to 95°C for 5 minutes and rapidly cool. If dissociating conditions are desired, add reducing agent prior to heating. The recommended loading volume per lane is 10-20 μl depending on the size format of your gel.
    Expiration Date12 months from date of receipt.
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