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DMGDH anticorps (C-Term)

Cet anticorps anti-DMGDH est un anticorps Lapin Polyclonal détectant DMGDH dans WB. Adapté pour Humain.
N° du produit ABIN1537626

Aperçu rapide pour DMGDH anticorps (C-Term) (ABIN1537626)

Antigène

Voir toutes DMGDH Anticorps
DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Reactivité

  • 30
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 30
Lapin

Clonalité

  • 30
Polyclonal

Conjugué

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DMGDH est non-conjugé

Application

  • 20
  • 17
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB23867
  • Épitope

    • 7
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    AA 836-864, C-Term

    Purification

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

    Immunogène

    This DMGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 836-864 amino acids from the C-terminal region of human DMGDH.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    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

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

    Date de péremption

    6 months
  • Antigène

    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

    Autre désignation

    DMGDH

    Sujet

    This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum.

    Poids moléculaire

    96811

    ID gène

    29958

    NCBI Accession

    NP_037523

    UniProt

    Q9UI17
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