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    H2AFY antibody

    Catalog Number: orb341227

    DispatchUsually dispatched within 5-10 working days
    $ 413.00
    Catalog Numberorb341227
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to H2AFY
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenRecombinant full length protein of human MacroH2A1
    Dilution rangeWB: 1:500-1:2000, IHC-P: 1:50-1:200, IF/ICC: 1:50-1:100
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetH2AFY
    Entrez26914, 29384, 9555
    UniProt IDQ9QZQ8, O75367, Q02874
    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 namesMACROH2A1; Core histone macro-H2A.1; Histone macro
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    H2AFY antibody

    Western blot analysis of MacroH2A1 expression in Jurkat (A), Hela (B), mouse liver (C), rat lung (D) whole cell lysates. (Predicted band size: 39 kD; Observed band size: 40 kD)

    H2AFY antibody

    Immunohistochemical analysis of MacroH2A1 staining in human kidney 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.

    H2AFY antibody

    Immunofluorescent analysis of MacroH2A1 staining in U2OS 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 hidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.

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