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DMGDH Antikörper (C-Term)

DMGDH Reaktivität: Human WB Wirt: Kaninchen Polyclonal RB23867 unconjugated
Produktnummer ABIN1537626
  • Target Alle DMGDH Antikörper anzeigen
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Bindungsspezifität
    • 7
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    AA 836-864, C-Term
    Reaktivität
    • 30
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 30
    Kaninchen
    Klonalität
    • 30
    Polyklonal
    Konjugat
    • 15
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DMGDH Antikörper ist unkonjugiert
    Applikation
    • 20
    • 17
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    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.
    Klon
    RB23867
    Isotyp
    Ig Fraction
    Top Product
    Discover our top product DMGDH Primärantikörper
  • Applikationshinweise
    WB: 1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
    4 °C,-20 °C
    Informationen zur Lagerung
    DMGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    Haltbarkeit
    6 months
  • Target
    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
    Andere Bezeichnung
    DMGDH (DMGDH Produkte)
    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.
    Molekulargewicht
    96811
    Gen-ID
    29958
    NCBI Accession
    NP_037523
    UniProt
    Q9UI17
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