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alpha KGDHC anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-alpha KGDHC a été validé pour WB et IHC (p). Il convient pour détecter alpha KGDHC dans des échantillons de Humain.
N° du produit ABIN657365

Aperçu rapide pour alpha KGDHC anticorps (C-Term) (ABIN657365)

Antigène

Voir toutes alpha KGDHC (alphaKGDHC) Anticorps
alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))

Reactivité

  • 29
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 28
  • 3
Lapin

Clonalité

  • 28
  • 3
Polyclonal

Conjugué

  • 20
  • 3
  • 3
  • 3
  • 1
  • 1
Cet anticorp alpha KGDHC est non-conjugé

Application

  • 27
  • 19
  • 15
  • 7
  • 6
  • 6
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32469
  • Épitope

    • 7
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 381-410, C-Term

    Purification

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

    Immunogène

    This OGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 381-410 amino acids from the C-terminal region of human OGDH.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    OGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Date de péremption

    6 months
  • Antigène

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

    Autre désignation

    OGDH

    Sujet

    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.

    Poids moléculaire

    115935

    ID gène

    4967

    NCBI Accession

    NP_001003941, NP_001158508, NP_002532

    UniProt

    Q02218
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