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DPYD anticorps (AA 265-370)

DPYD Reactivité: Humain WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1387275
  • Antigène Voir toutes DPYD Anticorps
    DPYD (Dihydropyrimidine Dehydrogenase (DPYD))
    Épitope
    • 14
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-370
    Reactivité
    • 41
    • 14
    • 12
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 41
    • 2
    Lapin
    Clonalité
    • 40
    • 3
    Polyclonal
    Conjugué
    • 18
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp DPYD est non-conjugé
    Application
    • 31
    • 12
    • 12
    • 11
    • 7
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Homologie
    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human DPYD
    Isotype
    IgG
    Top Product
    Discover our top product DPYD Anticorps primaire
  • Indications d'application
    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    DPYD (Dihydropyrimidine Dehydrogenase (DPYD))
    Autre désignation
    Dpyd (DPYD Produits)
    Synonymes
    anticorps DPYD, anticorps dpyd, anticorps zgc:77205, anticorps AI315208, anticorps DPD, anticorps E330028L06Rik, anticorps DHP, anticorps DHPDHASE, anticorps dhp, anticorps dhpdhase, anticorps dpd, anticorps 14.t00017, anticorps DDBDRAFT_0189681, anticorps DDBDRAFT_0231100, anticorps DDB_0189681, anticorps DDB_0231100, anticorps dpyda, anticorps zgc:153505, anticorps dihydropyrimidine dehydrogenase, anticorps dihydropyrimidine dehydrogenase b, anticorps dihydropyrimidine dehydrogenase L homeolog, anticorps dihydropyrimidine dehydrogenase [NADP(+)], anticorps dihydropyrimidine dehydrogenase a, tandem duplicate 1, anticorps DPYD, anticorps Dpyd, anticorps dpydb, anticorps dpyd.L, anticorps EHI_012980, anticorps LOC5573038, anticorps EDI_044620, anticorps pyd1, anticorps dpyda.1
    Sujet

    Synonyms: DHP, DHPDHase, Dihydropyrimidine dehydrogenase [NADP+], Dihydropyrimidine dehydrogenase, Dihydrothymine dehydrogenase, Dihydrouracil dehydrogenase, DPD, DPYD, DPYD_HUMAN, MGC132008, MGC70799, OTTHUMP00000058954.

    Background: Dihydropyrimidine dehydrogenase (DPYD) catalyzes the first rate-limiting step of the NADPH-dependent catabolism of uracil and thymine to dihydrouracil and dihydrothymine, thus, a deficiency of DPYD leads to an accumulation of uracil and thymine. Abnormal concentrations of these metabolites in bodily fluids may be the cause of neurological disease and a contraindication for treatment of cancer patients with certain pyrimidine analogs. DPYD also catalyzes the anticancer agent 5-fluorouracil (5-FU) pathway and is involved in the efficacy and toxicity of 5-FU. Variations in DPYD concentration may arise from alterations at the transcriptional level of the dihydropyrimidine dehydrogenase gene. Specifically, hypermethylation of the DPYD promoter downregulates dihydropyrimidine dehydrogenase expression. Deficient DPYD alleles may constitute a risk factor for severe toxicity following treatment with 5-FU.Involvement in disease:Defects in DPYD are the cause of dihydropyrimidine dehydrogenase deficiency (DPYD deficiency) , 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.

    ID gène
    1806
    Pathways
    Ribonucleoside Biosynthetic Process
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