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    AKAP8 antibody

    Catalog Number: orb214972

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb214972
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to AKAP8
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Rat
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human AKAP8. The exact sequence is proprietary.
    Dilution rangeWB: 1-500-1-1000, IF/ICC: 1-100-1-500
    Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    ConjugationUnconjugated
    TargetAKAP8
    Entrez116633, 10270, 56399
    UniProt IDO43823, Q9DBR0, Q63014
    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 AKAP95 antibody, anti A-kinase anchor protein
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    AKAP8 antibody

    Western blot analysis of AKAP8 expression in HepG2 (A), Jurkat (B), mouse kidney (C), rat kidney (D) whole cell lysates. (Predicted band size: 76 kD; Observed band size: 95 kD)

    AKAP8 antibody

    Immunohistochemical analysis of AKAP8 staining in human heart 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.

    AKAP8 antibody

    Immunofluorescent analysis of AKAP8 staining in Jurkat 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.

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