Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Ataxin 1 antibody

The Rabbit Polyclonal anti-Ataxin 1 antibody has been validated for WB, IHC and ELISA. It is suitable to detect Ataxin 1 in samples from Mouse, Human and Rat.
Catalog No. ABIN7249019
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for Ataxin 1 antibody (ABIN7249019)

Target

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

Reactivity

  • 99
  • 61
  • 36
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse, Human, Rat

Host

  • 73
  • 61
  • 1
Rabbit

Clonality

  • 72
  • 63
Polyclonal

Conjugate

  • 49
  • 9
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 1 antibody is un-conjugated

Application

  • 97
  • 51
  • 48
  • 46
  • 35
  • 33
  • 23
  • 23
  • 9
  • 8
  • 6
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human ATXN1

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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 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.

    Molecular Weight

    87 kDa

    UniProt

    P54253

    Pathways

    Synaptic Membrane
You are here:
Chat with us!