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GLRB antibody (N-Term)

This anti-GLRB antibody is a Rabbit Polyclonal antibody detecting GLRB in WB. Suitable for Human.
Catalog No. ABIN5536519

Quick Overview for GLRB antibody (N-Term) (ABIN5536519)

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
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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
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  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
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    • 1
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    AA 103-132, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    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

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) 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 for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 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 kDa

    Gene ID

    2743

    UniProt

    P48167
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