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    NIPA antibody

    Catalog Number: orb315746

    DispatchUsually dispatched within 5-10 working days
    $ 337.00
    Catalog Numberorb315746
    CategoryAntibodies
    DescriptionRabbit polyclonal antibody to NIPA
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsIF, IH, WB
    ReactivityHuman, Mouse, Primate
    ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human NIPA. The exact sequence is proprietary.
    Dilution rangeWB: 1-500:1000, IHC-P: 1-100:200, 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
    TargetZC3HC1
    Entrez232679, 51530
    UniProt IDQ86WB0, Q80YV2
    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 NIPA antibody, anti Nuclear-interacting partn
    Read more...
    NoteFor research use only
    Expiration Date12 months from date of receipt.
    NIPA antibody

    Western blot analysis of NIPA expression in A375 (A), A2780 (B), HEK293T (C), U87MG (D) whole cell lysates. (Predicted band size: 55 kD; Observed band size: 65 kD)

    NIPA antibody

    Immunohistochemical analysis of NIPA staining in human breast cancer 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.

    NIPA antibody

    Immunofluorescent analysis of NIPA staining in HepG2 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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