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DMGDH anticorps

DMGDH Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7073738
  • Antigène Voir toutes DMGDH Anticorps
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Reactivité
    • 36
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 36
    Lapin
    Clonalité
    • 36
    Polyclonal
    Conjugué
    • 16
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp DMGDH est non-conjugé
    Application
    • 26
    • 22
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
     Réactivité croisée
    Humain
    Purification
    Affinity purification
    Immunogène
    Recombinantproteincorrespondingto Mouse DMGDH
    Top Product
    Discover our top product DMGDH Anticorps primaire
  • Indications d'application
    WB (H) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % 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
    -20 °C
  • Antigène
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Autre désignation
    DMGDH (DMGDH Produits)
    Synonymes
    anticorps MGC132281, anticorps DMGDHD, anticorps ME2GLYDH, anticorps Me2GlyDH, anticorps 1200014D15Rik, anticorps AI787269, anticorps dimethylglycine dehydrogenase, anticorps dimethylglycine dehydrogenase L homeolog, anticorps D-amino-acid oxidase, anticorps Dimethylglycine dehydrogenase, anticorps glycine cleavage system protein T, anticorps dimethylglycine dehydrogenase precursor, anticorps DMGDH, anticorps dmgdh.L, anticorps dmgdh, anticorps SAR11_1253, anticorps EAMY_RS27375, anticorps EAMY_RS33570, anticorps VDBG_06516, anticorps Sinme_2570, anticorps HALXA_RS03495, anticorps 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. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    97 kDa
    ID gène
    74129
    NCBI Accession
    NP_083048
    UniProt
    Q9DBT9
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