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DMGDH Antikörper

DMGDH Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7073738
  • Target Alle DMGDH Antikörper anzeigen
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Reaktivität
    • 36
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 36
    Kaninchen
    Klonalität
    • 36
    Polyklonal
    Konjugat
    • 16
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DMGDH Antikörper ist unkonjugiert
    Applikation
    • 26
    • 22
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Kreuzreaktivität
    Human
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinantproteincorrespondingto Mouse DMGDH
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  • Applikationshinweise
    WB (H) 1:500-1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
  • Target
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Andere Bezeichnung
    DMGDH (DMGDH Produkte)
    Synonyme
    MGC132281 antikoerper, DMGDHD antikoerper, ME2GLYDH antikoerper, Me2GlyDH antikoerper, 1200014D15Rik antikoerper, AI787269 antikoerper, dimethylglycine dehydrogenase antikoerper, dimethylglycine dehydrogenase L homeolog antikoerper, D-amino-acid oxidase antikoerper, Dimethylglycine dehydrogenase antikoerper, glycine cleavage system protein T antikoerper, dimethylglycine dehydrogenase precursor antikoerper, DMGDH antikoerper, dmgdh.L antikoerper, dmgdh antikoerper, SAR11_1253 antikoerper, EAMY_RS27375 antikoerper, EAMY_RS33570 antikoerper, VDBG_06516 antikoerper, Sinme_2570 antikoerper, HALXA_RS03495 antikoerper, Dmgdh antikoerper
    Hintergrund
    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.
    Molekulargewicht
    97 kDa
    Gen-ID
    74129
    NCBI Accession
    NP_083048
    UniProt
    Q9DBT9
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