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Torsin A Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
SDP

Catalog No. 501726187 Shop All Proteintech Group Inc Products
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50-172-6187 150 μL
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Catalog No. 50-172-6187 Supplier Proteintech Group Inc Supplier No. 102961AP150UL
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Rabbit Polyclonal Antibody

A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal domitly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins in childhood. Symptoms are believed to result from altered neuronal communication in the basal ganglia. TorsinA comprises 332 amino acids. TorsinA is widely expressed throughout the mouse central nervous system and is detected in the majority of neurons in nearly all regions. The proteins display cytoplasmic distribution, although in some types of neurons localization is perinuclear. TorsinA often performs chaperone-like functions that assist in the assembly, operation, or dis-assembly of protein complexes. The gene which encodes TorsinA has high homology to three additional mammalian genes and a nematode gene and distal similarity to the family of heat-shock proteins and the Clp protease family. The gene which encodes TorsinA maps to human chromosome 9q34.

Specifications

Antigen Torsin A
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 0.26 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.1% sodium azide; pH 7.3
Gene TOR1A
Gene Accession No. O14656, Q68G38, Q9ER39
Gene Alias DQ2, Dystonia 1 protein, DYT1, TOR1A, Torsin 1A, Torsin A, Torsin family 1 member A, TorsinA
Gene Symbols TOR1A
Host Species Rabbit
Immunogen Torsin A Fusion Protein Ag0358
Purification Method Antigen Affinity Chromatography
Quantity 150 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 1861, 266606, 30931
Target Species Human, Mouse, Rat
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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