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TOR1A antibody

TOR1A Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7270856
  • Target See all TOR1A Antibodies
    TOR1A (Torsin Family 1, Member A (Torsin A) (TOR1A))
    Reactivity
    • 51
    • 12
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 51
    • 1
    Rabbit
    Clonality
    • 50
    • 2
    Monoclonal
    Conjugate
    • 17
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This TOR1A antibody is un-conjugated
    Application
    • 38
    • 21
    • 13
    • 13
    • 8
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purpose
    TorsinA/TOR1A Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human TorsinA/TOR1A
    Isotype
    IgG
    Top Product
    Discover our top product TOR1A Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    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
    TOR1A (Torsin Family 1, Member A (Torsin A) (TOR1A))
    Alternative Name
    TOR1A (TOR1A Products)
    Synonyms
    Dyt1 antibody, DQ2 antibody, DYT1 antibody, torsinA antibody, torsin family 1, member A antibody, torsin family 1 member A antibody, torsin family 1, member A (torsin A) antibody, Tor1a antibody, TOR1A antibody
    Background
    The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family and is expressed prominently in the substantia nigra pars compacta. Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1. [provided by RefSeq, Jul 2008],DQ2, DYT1,Neurodegenerative Diseases,Neurodegenerative Diseases_Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimers Disease,Neurodegenerative Diseases_Dopamine Signaling in Parkinsons Disease,Neuroscience,TOR1A
    Molecular Weight
    35kDa
    Gene ID
    1861
    UniProt
    O14656
    Pathways
    SARS-CoV-2 Protein Interactome
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