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Ataxin 1 antibody (AA 350-400)

This Rabbit Polyclonal antibody specifically detects Ataxin 1 in IP. It exhibits reactivity toward Human.
Catalog No. ABIN7449649

Quick Overview for Ataxin 1 antibody (AA 350-400) (ABIN7449649)

Target

See all Ataxin 1 (ATXN1) Antibodies
Ataxin 1 (ATXN1)

Reactivity

  • 79
  • 63
  • 35
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 66
  • 52
  • 1
Rabbit

Clonality

  • 66
  • 53
Polyclonal

Conjugate

  • 50
  • 8
  • 7
  • 7
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 1 antibody is un-conjugated

Application

  • 89
  • 45
  • 44
  • 36
  • 34
  • 24
  • 23
  • 23
  • 9
  • 6
  • 6
  • 1
  • 1
Immunoprecipitation (IP)
  • Binding Specificity

    • 28
    • 22
    • 17
    • 12
    • 7
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 350-400

    Purpose

    Rabbit anti-Ataxin-1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 350 and 400

    Isotype

    IgG
  • Application Notes

    IP: 10 μg/mg lysate

    WB: Not recommended. Use rabbit anti-Ataxin-1 antibody A302-292A.

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    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

    4 °C

    Expiry Date

    12 months
  • Target

    Ataxin 1 (ATXN1)

    Alternative Name

    Ataxin-1

    Background

    Background: Defects in ataxin-1 are the cause of spinocerebellar ataxia type 1 (SCA1), also known as olivopontocerebellar atrophy I (OPCA I or OPCA1). Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to cerebellum degeneration with variable involvement of the brainstem and spinal cord. SCA1 is caused by expansion of a CAG repeat in the coding region of the ataxin-1 gene. Longer expansions result in earlier onset and more severe clinical manifestations of the disease. Ataxin-1 binds RNA in vitro and may be involved in RNA metabolism [taken from the Universal Protein Resource (UniProt) P54253].

    Gene ID

    6310

    NCBI Accession

    NP_000323

    UniProt

    P54253

    Pathways

    Synaptic Membrane
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