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Western Blot analysis of 293T cell and Human fetal brain tissue using ATXN1 Polyclonal Antibody at dilution of 1:800
Western Blot analysis of 293T cell and Human fetal brain tissue using ATXN1 Polyclonal Antibody at dilution of 1:800
Western Blot analysis of 293T cell and Human fetal brain tissue using ATXN1 Polyclonal Antibody at dilution of 1:800

ATXN1 Polyclonal Antibody

E-AB-14779
Elabscience
Product group Antibodies
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Overview

  • Supplier
    Elabscience
  • Product Name
    ATXN1 Polyclonal Antibody
  • Delivery Days Customer
    12
  • Applications Supplier
    ELISA WB IHC
  • Certification
    Research Use Only
  • Concentration
    0.3mg/ml
  • Scientific Description
    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.
  • UNSPSC
    12352203