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GLRB antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects GLRB in WB. It exhibits reactivity toward Human.
Catalog No. ABIN2798821

Quick Overview for GLRB antibody (N-Term) (ABIN2798821)

Target

See all GLRB Antibodies
GLRB (Glycine Receptor, beta (GLRB))

Reactivity

  • 34
  • 28
  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 40
  • 1
Rabbit

Clonality

  • 40
  • 1
Polyclonal

Conjugate

  • 13
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLRB antibody is un-conjugated

Application

  • 30
  • 17
  • 13
  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

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

    Purpose

    Rabbit Anti-Human GLRB (N-term) Antibody

    Immunogen

    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
  • Application Notes

    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

    Storage

    4 °C,-20 °C

    Storage Comment

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

    GLRB (Glycine Receptor, beta (GLRB))

    Alternative Name

    GLRB

    Background

    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

    Molecular Weight

    56122 Da

    Gene ID

    2743

    UniProt

    P48167
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