TOR1A polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS6589
Background:
A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly 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.
Alternative Name:
DQ2, Dystonia 1, Dystonia 1 protein, Dystonia 1 torsion, Dyt1, Tor1a, Torsin 1A, Torsin A, Torsin family 1 member A, Torsin family 1, member A (torsin A),
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: TOR1A polyclonal antibody detects endogenous levels of TOR1A protein.
Immunogen:
Recombinant full length Human TOR1A.
MW: ~ 38 kDa
Swis Prot.: O14656
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly 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.
Alternative Name:
DQ2, Dystonia 1, Dystonia 1 protein, Dystonia 1 torsion, Dyt1, Tor1a, Torsin 1A, Torsin A, Torsin family 1 member A, Torsin family 1, member A (torsin A),
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: TOR1A polyclonal antibody detects endogenous levels of TOR1A protein.
Immunogen:
Recombinant full length Human TOR1A.
MW: ~ 38 kDa
Swis Prot.: O14656
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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