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Ataxin 3 antibody

This anti-Ataxin 3 antibody is a Rabbit Polyclonal antibody detecting Ataxin 3 in WB and IF. Suitable for Human and Mouse.
Catalog No. ABIN6567724

Quick Overview for Ataxin 3 antibody (ABIN6567724)

Target

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

Reactivity

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Human, Mouse

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)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human ATXN3

    Isotype

    IgG
  • Application Notes

    WB 1:500 - 1:2000 IF 1:50 - 1:200

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Ataxin 3 (ATXN3)

    Alternative Name

    ATXN3

    Background

    Synonyms: AT3,Ataxin 3,ataxin 3 variant h,ataxin 3 variant m,ataxin 3 variant ref,Ataxin-3,ATX3,ATX3,ATXN3,EC 3.4.22.,JOS,Josephin,Machado Joseph disease (spinocerebellar ataxia 3,olivopontocerebellar ataxia 3,autosomal dominant,ataxin 3),Machado Joseph disease,Machado Joseph disease protein 1,Machado-Joseph disease protein 1,Machado-Joseph disease protein 1 homolog,MJD,MJD gene,MJD1,Olivopontocerebellar ataxia 3,OTTHUMP00000221583,OTTHUMP00000221585,OTTHUMP00000221586,OTTHUMP00000221587,OTTHUMP00000231995,OTTHUMP00000231997,Rsca3,SCA3,SCA3 gene,Spinocerebellar ataxia type 3 protein

    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 12-44 to 52-86 is one 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.

    Molecular Weight

    Observed_MW: 50kDa

    Calculated_MW: 20kDa/35kDa/39kDa/41kDa

    Gene ID

    4287

    UniProt

    P54252
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