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GCDH antibody

The Rabbit Polyclonal anti-GCDH antibody (ABIN7004050) specifically detects GCDH in IHC and ELISA. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7004050
-15% Promotion 2026
$121.38
$142.80
save $21.42 (-15 %)
Plus shipping costs $50.00
20 μL
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for GCDH antibody (ABIN7004050)

Target

See all GCDH Antibodies
GCDH (Glutaryl-CoA Dehydrogenase (GCDH))

Reactivity

  • 58
  • 13
  • 10
  • 7
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
Human, Mouse

Host

  • 57
  • 3
Rabbit

Clonality

  • 60
Polyclonal

Conjugate

  • 31
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GCDH antibody is un-conjugated

Application

  • 49
  • 19
  • 18
  • 13
  • 13
  • 8
  • 5
  • 5
  • 5
  • 3
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human GCDH

    Isotype

    IgG
  • Application Notes

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.02 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))

    Alternative Name

    GCDH

    Background

    The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12.

    UniProt

    Q92947
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