Catalog No.
RHA26102
Species reactivity
Human
Host species
Rabbit
Isotype
IgG
Clonality
Monoclonal
Tested applications
FCM: 1:20-1:100, WB: 1:1000-1:2000
Target
TOR1A, DQ2, DYT1, TorsinA, Torsin 1A
Concentration
1 mg/ml
Endotoxin level
Please contact with the lab for this information.
Purity
>95% by SDS-PAGE.
Purification
Protein A/G purified from cell culture supernatant.
Accession
O14656
Applications
FCM, WB
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4, 0.05% BSA, 50% Glycerol, 0.05% Sodium azide.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
Store at +4 ℃ short term (1-2 weeks).
Store at -20 ℃ 12 months.
Store at -80 ℃ long term.
Clone ID
R1A84
A2A Receptor Dysregulation in Dystonia DYT1 Knock-Out Mice., PMID:33799994
Dystonia: Sparse Synapses for D2 Receptors in Striatum of a DYT1 Knock-out Mouse Model., PMID:32041188
The possible link between coeliac and Kawasaki diseases in Brazil: a cross-sectional study., PMID:29444780
Phosphodiesterase-10A Inverse Changes in Striatopallidal and Striatoentopeduncular Pathways of a Transgenic Mouse Model of DYT1 Dystonia., PMID:28115486
Dystonia type 6 gene product Thap1: identification of a 50 kDa DNA-binding species in neuronal nuclear fractions., PMID:25231164
Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons., PMID:24025868
Allelic Imbalance in TOR1A mRNA Expression in Manifesting and Non-Manifesting Carriers of the GAG-Deletion., PMID:22988486
Transglutaminase 2-targeted autoantibodies in celiac disease: Pathogenetic players in addition to diagnostic tools?, PMID:20547248
Transient expression of human TorsinA enhances secretion of two functionally distinct proteins in cultured Chinese hamster ovary (CHO) cells., PMID:19845036
The dystonia-associated protein torsinA modulates synaptic vesicle recycling., PMID:18167355
Stiff child syndrome with mutation of DYT1 gene., PMID:16682692
Silencing primary dystonia: lentiviral-mediated RNA interference therapy for DYT1 dystonia., PMID:16280588
Stiff child syndrome with mutation of DYT1 gene., PMID:16275837
Torsin-mediated protection from cellular stress in the dopaminergic neurons of Caenorhabditis elegans., PMID:15829632
Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells., PMID:15593317
TorsinB--perinuclear location and association with torsinA., PMID:15147511
TorsinA immunoreactivity in inclusion bodies in trinucleotide repeat diseases., PMID:14502672
Distribution and ultrastructural localization of torsinA immunoreactivity in the human brain., PMID:12965225
Suppression of polyglutamine-induced protein aggregation in Caenorhabditis elegans by torsin proteins., PMID:12554684
Immunocytochemical characterization of torsin proteins in mouse brain., PMID:11730696
A close association of torsinA and alpha-synuclein in Lewy bodies: a fluorescence resonance energy transfer study., PMID:11438481
Cellular distribution of torsin A and torsin B in normal human brain., PMID:11405807
Distribution and immunohistochemical characterization of torsinA immunoreactivity in rat brain., PMID:11334819
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells., PMID:10814722
Immunohistochemical localization and distribution of torsinA in normal human and rat brain., PMID:10640617
For research use only. Not for human or drug use.
