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Ataxin 3 antibody (AA 1-215)

This Rabbit Polyclonal antibody specifically detects Ataxin 3 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN1885789

Quick Overview for Ataxin 3 antibody (AA 1-215) (ABIN1885789)

Target

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

Reactivity

  • 57
  • 31
  • 30
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 54
  • 2
  • 1
Rabbit

Clonality

  • 56
  • 1
Polyclonal

Conjugate

  • 25
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 3 antibody is un-conjugated

Application

  • 45
  • 21
  • 19
  • 13
  • 13
  • 11
  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 8
    • 7
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-215

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 215 of Ataxin 3
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • 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.[provided by RefSeq]

    Molecular Weight

    42 kDa

    Gene ID

    4287
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