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    IL-32A antibody

    Catalog Number: orb345133

    DispatchUsually dispatched within 5-10 working days
    $ 784.00
    Catalog Numberorb345133
    CategoryAntibodies
    DescriptionIL-32A antibody
    Species/HostRabbit
    ClonalityPolyclonal
    Tested applicationsELISA, WB
    ReactivityHuman
    IsotypeIgG
    ImmunogenThis purified antibody was prepared from whole rabbit serum produced by repeated immunizations with full length recombinant human IL-32A protein.
    Concentration1.0 mg/mL
    Dilution rangeELISA: 1:20,000 - 1:100,000, WB: 1:500 - 1:2,000
    Form/AppearanceLyophilized
    PurityThis purified antibody has been heated to 56°C for 30 minutes. In ELISA and other immunoreactive assays, this antibody will recognize both native and recombinant human IL-32A in cell supernatants and certain body fluids. A control of similarly diluted normal rabbit IgG is recommended.
    ConjugationUnconjugated
    UniProt IDP24001
    NCBI61658634
    StorageStore vial at 4° C prior to restoration. For extended storage aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.
    Buffer/PreservativesNone
    Alternative namesrabbit anti-IL-32A antibody, rabbit anti-interleuk
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    NoteFor research use only
    Application notesThis purified antibody has been tested in western blotting. Reactivity is also expected in ELISA, neutralizations, radioimmunoassay and immunohistochemistry. The endotoxin content is estimated to be < 10 pg/µl by the LAL method. By western blot a band approximately 15 kDa in size corresponding to native human IL-32α protein is expected in the appropriate cell lysate or extract. Specific conditions for reactivity should be optimized by the end user.
    Expiration Date12 months from date of receipt.
    IL-32A antibody

    Western blot analysis of (lane 1). The identity of the higher molecular weight band is unknown. Molecular weight markers are also shown (M). After transfer, the membrane was blocked overnight with 3% BSA in TBS followed by reaction with primary antibody a

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