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Ataxin 3 antibody

The Rabbit Polyclonal anti-Ataxin 3 antibody has been validated for WB, IF, IP and ICC. It is suitable to detect Ataxin 3 in samples from Human.
Catalog No. ABIN2854322

Quick Overview for Ataxin 3 antibody (ABIN2854322)

Target

See all Ataxin 3 (ATXN3) Antibodies
Ataxin 3 (ATXN3)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Ataxin 3 antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunocytochemistry (ICC)

Grade

KO Validated
  • Cross-Reactivity

    Human

    Characteristics

    Rabbit Polyclonal antibody to Ataxin 3 (ataxin-3)
    Ataxin 3 antibody

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Ataxin 3. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:20000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: SK-N-SH , SK-N-AS , human Ataxin3-transfected 293T , 293T , A431 , HeLa , HepG2

    Validation: KO/KD, Overexpression

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.55 mg/mL

    Buffer

    1XPBS ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Ataxin 3 (ATXN3)

    Alternative Name

    ataxin 3

    Background

    Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by this gene contains (CAG)n repeats in the coding region, and the expansion of these repeats from the normal 13-36 to 68-79 is the cause of Machado-Joseph disease. There is a negative correlation between the age of onset and CAG repeat numbers. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

    Cellular Localization: Nucleus matrix

    Molecular Weight

    42 kDa

    Gene ID

    4287

    UniProt

    P54252
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