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GLRA1 anticorps (AA 29-154)

GLRA1 Reactivité: Humain ELISA Hôte: Souris Monoclonal 7F8E2 unconjugated
N° du produit ABIN5611339
  • Antigène Voir toutes GLRA1 Anticorps
    GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
    Épitope
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 29-154
    Reactivité
    • 30
    • 16
    • 16
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 28
    • 3
    • 1
    Souris
    Clonalité
    • 28
    • 3
    Monoclonal
    Conjugué
    • 21
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GLRA1 est non-conjugé
    Application
    • 20
    • 11
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    ELISA
    Fonction
    GLRA1 Antibody
    Purification
    Purified antibody
    Immunogène
    Purified recombinant fragment of human GLRA1 (AA: 29-154) expressed in E. Coli.
    Clone
    7F8E2
    Isotype
    IgG1
    Top Product
    Discover our top product GLRA1 Anticorps primaire
  • Indications d'application
    ELISA: 1/10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified antibody in PBS with 0.05 % sodium azide.
    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
    4 °C,-20 °C
    Stockage commentaire
    Store at 4°C short term. Aliquot and store at -20°C long term. 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

    Description: The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which 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. Multiple transcript variants encoding different isoforms have been found.

    Aliases: STHE, HKPX1

    Poids moléculaire
    52.6kDa
    ID gène
    2741
    HGNC
    2741
    Pathways
    Synaptic Membrane
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