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Ataxin 1 antibody

This anti-Ataxin 1 antibody is a Mouse Monoclonal antibody detecting Ataxin 1 in WB, IHC, ELISA, IF and FACS. Suitable for Human.
Catalog No. ABIN865485

Quick Overview for Ataxin 1 antibody (ABIN865485)

Target

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

Reactivity

  • 85
  • 59
  • 36
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 71
  • 48
  • 1
Mouse

Clonality

  • 62
  • 58
Monoclonal

Conjugate

  • 42
  • 9
  • 7
  • 7
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 1 antibody is un-conjugated

Application

  • 90
  • 41
  • 40
  • 33
  • 33
  • 31
  • 23
  • 23
  • 7
  • 7
  • 6
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

2F5
  • Purification

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human ATXN1 expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, IF: 1/200 - 1/1000, FC: 1/200-1/400 ELISA: Propose dilution 1/10000. Figure 3: Immunofluorescence

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    100g/100l

    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
  • Target

    Ataxin 1 (ATXN1)

    Alternative Name

    ATXN1

    Background

    The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. Synonyms: ATX1, SCA1, D6S504E, ATXN1

    Molecular Weight

    87kDa

    Gene ID

    6310

    Pathways

    Synaptic Membrane
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