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GLRA1 antibody

GLRA1 Reactivity: Human, Mouse, Rat WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7242839
  • Target See all GLRA1 Antibodies
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    Reactivity
    • 30
    • 15
    • 15
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 27
    • 4
    • 1
    Rabbit
    Clonality
    • 27
    • 4
    Polyclonal
    Conjugate
    • 21
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GLRA1 antibody is un-conjugated
    Application
    • 19
    • 11
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human GLRA1
    Isotype
    IgG
    Top Product
    Discover our top product GLRA1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:25-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.2 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    Alternative Name
    GLRA1 (GLRA1 Products)
    Synonyms
    GLYRA1 antibody, HKPX1 antibody, STHE antibody, [a]Z1 antibody, B230397M16Rik antibody, nmf11 antibody, oscillator antibody, ot antibody, spasmodic antibody, spd antibody, glycine receptor alpha 1 antibody, glycine receptor, alpha 1 antibody, glycine receptor, alpha 1 subunit antibody, GLRA1 antibody, Glra1 antibody, glra1 antibody
    Background
    The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    53 kDa
    NCBI Accession
    NP_000162
    UniProt
    P23415
    Pathways
    Synaptic Membrane
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