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GLRB antibody (AA 23-160)

This Mouse Monoclonal antibody specifically detects GLRB in ELISA, ICC and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN5611340

Quick Overview for GLRB antibody (AA 23-160) (ABIN5611340)

Target

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

Reactivity

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

Host

  • 41
Mouse

Clonality

  • 41
Monoclonal

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

  • 31
  • 16
  • 13
  • 13
  • 3
  • 3
  • 1
  • 1
  • 1
ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

3B8A8
  • Binding Specificity

    • 15
    • 9
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 23-160

    Purpose

    GLRB Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human GLRB (AA: 23-160) expressed in E. Coli.

    Isotype

    IgG2b
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    GLRB (Glycine Receptor, beta (GLRB))

    Alternative Name

    GLRB

    Background

    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.

    Molecular Weight

    56.1 kDa

    Gene ID

    2743

    UniProt

    P48167
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