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    FGF22 antibody

    Catalog Number: orb393288

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb393288
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to FGF22.
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human FGF22. The exact sequence is proprietary.
    Dilution rangeWB: 1:500:1000, IF/ICC: 1:100:500
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetFGF22
    Entrez67112, 27006
    UniProt IDQ9ESS2, Q9HCT0
    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 namesFibroblast growth factor 22; FGF-22
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    FGF22 antibody

    Western blot analysis of FGF22 expression in rat skin (A), HEK293T (B), BV2 (C) whole cell lysates. (Predicted band size: 19 kD; Observed band size: 20 kD)

    FGF22 antibody

    Immunohistochemical analysis of FGF22 staining in human ovary 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.

    FGF22 antibody

    Immunofluorescent analysis of FGF22 staining in K562 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. DAPI was used to stain the cell nuclei (blue).

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