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alpha KGDHC antibody

This Rabbit Polyclonal antibody specifically detects alpha KGDHC in WB, IHC, ELISA and IF. It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN7111489

Quick Overview for alpha KGDHC antibody (ABIN7111489)

Target

See all alpha KGDHC (alphaKGDHC) Antibodies
alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))

Reactivity

  • 30
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 29
  • 3
Rabbit

Clonality

  • 29
  • 3
Polyclonal

Conjugate

  • 21
  • 3
  • 3
  • 3
  • 1
  • 1
This alpha KGDHC antibody is un-conjugated

Application

  • 28
  • 19
  • 14
  • 8
  • 7
  • 5
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))

    Alternative Name

    OGDH

    Background

    Synonyms:AKGDH Background:This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Molecular Weight

    116 kDa

    Gene ID

    4967

    UniProt

    Q02218
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