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DMGDH anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement DMGDH dans WB et ELISA. Il présente une réactivité envers Humain.
N° du produit ABIN7180160

Aperçu rapide pour DMGDH anticorps (C-Term) (ABIN7180160)

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
  • 16
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 8
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    C-Term

    Fonction

    DMGDH Antibody

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from C-terminal of Human DMGDH.

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 0.02 % sodium azide and 50 % glycerol.

    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

    -20 °C,-80 °C

    Stockage commentaire

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène

    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

    Autre désignation

    DMGDH

    Sujet

    Background: 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. Alternative splicing results in multiple transcript variants.

    Binzak B.A., Mol. Genet. Metab. 69:181-187(2000).
    Binzak B.A., Am. J. Hum. Genet. 68:839-847(2001).
    Moolenaar S.H., Clin. Chem. 45:459-464(1999)

    Aliases: Dimethylglycine dehydrogenase antibody, Dimethylglycine dehydrogenase, mitochondrial antibody, Dmgdh antibody, M2GD_HUMAN antibody, ME2GLYDH antibody, mitochondrial antibody

    UniProt

    Q9UI17
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