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    Histone H2A.V antibody

    Catalog Number: orb666861

    DispatchUsually dispatched within 5-10 working days
    $ 413.00
    Catalog Numberorb666861
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to Histone H2A.V
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenRecombinant fusion protein of human Histone H2A.V. The exact sequence is proprietary.
    Dilution rangeWB: 1-500-2000
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetH2AFV
    Entrez77605, 94239
    UniProt IDQ3THW5, Q71UI9
    SourceRabbit
    StorageShipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
    Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    Alternative namesAnti-H2AV antibody, anti-Histone H2A.V antibody, a
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    Histone H2A.V antibody

    Western blot analysis of Histone H2A.V expression in A431 (A), mouse spleen (B), rat thymus (C), rat lung (D) whole cell lysates. (Predicted band size: 13 kD; Observed band size: 14 kD)

    Histone H2A.V antibody

    Immunohistochemical analysis of Histone H2A.V staining in rat testis formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

    Histone H2A.V antibody

    Immunofluorescent analysis of Histone H2A.V staining in C6 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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