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Recombinant Human Dihydropyrimidine dehydrogenase [NADP (+)] (DPYD), Truncated

ACP17888

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP17888 Target NameDPYD
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Protein LengthPartialPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ12882
Background Information
  • Uniprot Id

    Q12882

  • Target Species

    Human

  • Target Name

    DPYD

  • Target Full Name

    Dihydropyrimidine dehydrogenase [NADP(+)]

  • Target Function

    Involved in pyrimidine base degradation. Catalyzes the reduction of uracil and thymine. Also involved the degradation of the chemotherapeutic drug 5-fluorouracil.

  • Target Involvement

    Dihydropyrimidine dehydrogenase deficiency (DPYDD)

  • Target Subcellular Location

    Cytoplasm.

  • Target Protein Families

    Dihydropyrimidine dehydrogenase family

  • Target Tissue Specificity

    Found in most tissues with greatest activity found in liver and peripheral blood mononuclear cells.

  • Target Synonyms

    DHP; DHPDHase; Dihydropyrimidine dehydrogenase [NADP(+)]; Dihydropyrimidine dehydrogenase [NADP+]; Dihydropyrimidine dehydrogenase; Dihydrothymine dehydrogenase; Dihydrouracil dehydrogenase; DPD; DPYD; DPYD_HUMAN; MGC132008; MGC70799; OTTHUMP00000058954

  • Target Background

    The protein encoded by this gene is a pyrimidine catabolic enzyme and the initial and rate-limiting factor in the pathway of uracil and thymidine catabolism. Mutations in this gene result in dihydropyrimidine dehydrogenase deficiency, an error in pyrimidine metabolism associated with thymine-uraciluria and an increased risk of toxicity in cancer patients receiving 5-fluorouracil chemotherapy. Two transcript variants encoding different isoforms have been found for this gene.

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