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GLRB anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement GLRB dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN2798821

Aperçu rapide pour GLRB anticorps (N-Term) (ABIN2798821)

Antigène

Voir toutes GLRB Anticorps
GLRB (Glycine Receptor, beta (GLRB))

Reactivité

  • 33
  • 27
  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 39
  • 1
Lapin

Clonalité

  • 39
  • 1
Polyclonal

Conjugué

  • 12
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GLRB est non-conjugé

Application

  • 29
  • 16
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 8
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 103-132, N-Term

    Fonction

    Rabbit Anti-Human GLRB (N-term) Antibody

    Immunogène

    This GLRB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 103-132 amino acids from the N-terminal region of human GLRB.

    Isotype

    Ig Fraction
  • Indications d'application

    Western Blot
    Recommended Dilutions
    WB: 1:1000Western blot analysis of lysate from Jurkat cell line, using GLRB Antibody (N-term) at 1:5000 dilution was used as the secondary antibody. Lysate at 35 μg per lane.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Stock

    4 °C,-20 °C

    Stockage commentaire

    2-8°C (short-term), -20°C (long-term)
  • Antigène

    GLRB (Glycine Receptor, beta (GLRB))

    Autre désignation

    GLRB

    Sujet

    Target Description: This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants.

    Gene Symbol: GLRB

    Poids moléculaire

    56122 Da

    ID gène

    2743

    UniProt

    P48167
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