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DMGDH Antikörper (C-Term)

Dieses Anti-DMGDH-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von DMGDH in WB. Geeignet für Human.
Produktnummer ABIN1537626

Kurzübersicht für DMGDH Antikörper (C-Term) (ABIN1537626)

Target

Alle DMGDH Antikörper anzeigen
DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Reaktivität

  • 31
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 31
Kaninchen

Klonalität

  • 31
Polyklonal

Konjugat

  • 16
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DMGDH Antikörper ist unkonjugiert

Applikation

  • 21
  • 18
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB)

Klon

RB23867
  • Bindungsspezifität

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

    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.

    Isotyp

    Ig Fraction
  • 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

    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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