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GLRA1 anticorps

GLRA1 Reactivité: Humain, Souris, Rat WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7242839
  • Antigène Voir toutes GLRA1 Anticorps
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    Reactivité
    • 30
    • 15
    • 15
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 27
    • 4
    • 1
    Lapin
    Clonalité
    • 27
    • 4
    Polyclonal
    Conjugué
    • 21
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GLRA1 est non-conjugé
    Application
    • 19
    • 11
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human GLRA1
    Isotype
    IgG
    Top Product
    Discover our top product GLRA1 Anticorps primaire
  • Indications d'application
    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
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    Autre désignation
    GLRA1 (GLRA1 Produits)
    Synonymes
    anticorps GLYRA1, anticorps HKPX1, anticorps STHE, anticorps [a]Z1, anticorps B230397M16Rik, anticorps nmf11, anticorps oscillator, anticorps ot, anticorps spasmodic, anticorps spd, anticorps glycine receptor alpha 1, anticorps glycine receptor, alpha 1, anticorps glycine receptor, alpha 1 subunit, anticorps GLRA1, anticorps Glra1, anticorps glra1
    Sujet
    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.
    Poids moléculaire
    53 kDa
    NCBI Accession
    NP_000162
    UniProt
    P23415
    Pathways
    Synaptic Membrane
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