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Atrophin 1 antibody

This Rabbit Polyclonal antibody specifically detects Atrophin 1 in ELISA and IHC. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7254694

Quick Overview for Atrophin 1 antibody (ABIN7254694)

Target

See all Atrophin 1 (ATN1) Antibodies
Atrophin 1 (ATN1)

Reactivity

  • 26
  • 17
  • 8
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 23
  • 3
  • 1
Rabbit

Clonality

  • 24
  • 3
Polyclonal

Conjugate

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Atrophin 1 antibody is un-conjugated

Application

  • 20
  • 8
  • 6
  • 5
  • 5
  • 2
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human ATN1

    Isotype

    IgG
  • Application Notes

    IHC 1:40-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.9 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    Atrophin 1 (ATN1)

    Alternative Name

    ATN1

    Background

    Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein.ATN1 (Atrophin 1) is a Protein Coding gene. Diseases associated with ATN1 include Dentatorubro-Pallidoluysian Atrophy and Spinocerebellar Ataxia 1. GO annotations related to this gene include protein domain specific binding. An important paralog of this gene is RERE.

    UniProt

    P54259
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