Overview

Description

  • Nature
    Recombinant
  • Source
    Wheat germ
  • Amino Acid Sequence
    • Accession
    • Species
      Human
    • Sequence
      MAPVLSKDSADIESILALNPRTQTHATLCSTSAKKLDKKHWKRNPDKNCF NCEKLENNFDDIKHTTLGERGALREAMRCLKCADAPCQKSCPTNLDIKSF ITSIANKNYYGAAKMIFSDNPLGLTCGMVCPTSDLCVGGCNLYATEEGPI NIGGLQQFATETLILAFSLMNHL
    • Molecular weight
      45 kDa including tags
    • Amino acids
      1 to 173

Associated products

Specifications

Our Abpromise guarantee covers the use of ab114584 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    ELISA

    SDS-PAGE

    Western blot

  • Form
    Liquid
  • Additional notes
    Protein concentration is above or equal to 0.05 µg/ul. Best use within three months from the date of receipt of this protein.
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

General Info

  • Alternative names
    • DHP
    • DHPDHase
    • Dihydropyrimidine dehydrogenase
    • Dihydropyrimidine dehydrogenase [NADP(+)]
    • Dihydropyrimidine dehydrogenase [NADP+]
    • Dihydrothymine dehydrogenase
    • Dihydrouracil dehydrogenase
    • DPD
    • DPYD
    • DPYD_HUMAN
    • MGC132008
    • MGC70799
    • OTTHUMP00000058954
    see all
  • Function
    Involved in pyrimidine base degradation. Catalyzes the reduction of uracil and thymine. Also involved the degradation of the chemotherapeutic drug 5-fluorouracil.
  • Tissue specificity
    Found in most tissues with greatest activity found in liver and peripheral blood mononuclear cells.
  • Pathway
    Amino-acid biosynthesis; beta-alanine biosynthesis.
  • Involvement in disease
    Defects in DPYD are the cause of dihydropyrimidine dehydrogenase deficiency (DPYD deficiency) [MIM:274270]; also known as hereditary thymine-uraciluria or familial pyrimidinemia. DPYD deficiency is a disease characterized by persistent urinary excretion of excessive amounts of uracil, thymine and 5-hydroxymethyluracil. Patients suffering from this disease show a severe reaction to the anticancer drug 5-fluorouracil. This reaction includes stomatitis, Leukopenia, thrombocytopenia, hair loss, diarrhea, fever, marked weight loss, cerebellar ataxia, and neurologic symptoms, progressing to semicoma.
  • Sequence similarities
    Belongs to the dihydropyrimidine dehydrogenase family.
    Contains 3 4Fe-4S ferredoxin-type domains.
  • Cellular localization
    Cytoplasm.
  • Information by UniProt

Recombinant Human DPYD protein images

  • 12.5% SDS-PAGE showing ab114584 at approximately 45.03kDa stained with Coomassie Blue.

References for Recombinant Human DPYD protein (ab114584)

ab114584 has not yet been referenced specifically in any publications.

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