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DPYD antibody (N-Term)

This anti-DPYD antibody is a Rabbit Polyclonal antibody detecting DPYD in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN3044151

Quick Overview for DPYD antibody (N-Term) (ABIN3044151)

Target

See all DPYD Antibodies
DPYD (Dihydropyrimidine Dehydrogenase (DPYD))

Reactivity

  • 47
  • 16
  • 13
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 46
  • 4
Rabbit

Clonality

  • 45
  • 5
Polyclonal

Conjugate

  • 25
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DPYD antibody is un-conjugated

Application

  • 38
  • 14
  • 13
  • 13
  • 10
  • 7
  • 7
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 33-52, N-Term

    Purpose

    Anti-DPYD Antibody Picoband®

    Sequence

    AKKLDKKHWK RNPDKNCFNC

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Characteristics

    Anti-DPYD Antibody (ABIN3044151). Tested in WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    A synthetic peptide corresponding to a sequence at the N-terminus of human DPYD, different from the related rat and mouse sequences by one amino acid.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.1-0.5 μg/mL, Human, Mouse, Rat
    1. Albin, N., Johnson, M. R., Shahinian, H., Wang, K., Diasio, R. B. Initial characterization of the molecular defect in human dihydropyrimidine dehydrogenase deficiency. Proc. Am. Assoc. Cancer Res. (Abstract) 36: 211 only, 1995. 2. McLeod, H. L., Collie-Duguid, E. S. R., Vreken, P., Johnson, M. R., Wei, X., Sapone, A., Diasio, R. B., Fernandez-Salguero, P., van Kuilenberg, A. B. P., van Gennip, A. H., Gonzales, F. J. Nomenclature for human DPYD alleles. Pharmacogenetics 8: 455-459, 1998. 3. Ridge, S. A., Brown, O., McMurrough, J., Fernandez-Salguero, P., Evans, W. E., Gonzalez, F. J., McLeod, H. L. Mutations at codon 974 of theDPYD gene are a rare event. Brit. J. Cancer 75: 178-179, 1997.

    Comment

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Thimerosal, 0.05 mg Sodium azide.

    Preservative

    Thimerosal (Merthiolate), Sodium azide

    Precaution of Use

    This product contains Thimerosal (Merthiolate) and Sodium azide: POISONOUS AND HAZARDOUS SUBSTANCES which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    DPYD (Dihydropyrimidine Dehydrogenase (DPYD))

    Alternative Name

    DPYD

    Background

    Synonyms: Dihydropyrimidine dehydrogenase [NADP (+)],DHPDHase,DPD,1.3.1.2,Dihydrothymine dehydrogenase,Dihydrouracil dehydrogenase,DPYD,

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

    Background: DPYD (Dihydropyrimidine Dehydrogenase), also called DPD, is an enzyme that in humans is encoded by the DPYD gene. 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. The structure of the DPYD gene contains 23 exons spanning about 950 kb. Using somatic cell hybrid strategies, the DPYD gene is mapped to the centromeric region of chromosome 1 between 1p22 and 1q21. By fluorescence in situ hybridization, the DPYD gene is mapped to 1p22. The highest level of DPD was found in monocytes followed by that in lymphocytes, granulocytes, and platelets, whereas no significant activity of DPD could be detected in erythrocytes. The activity of DPD in peripheral blood mononuclear cells was intermediate between that observed in monocytes and lymphocytes. By cDNA microarray, Western blot analysis, and luciferase reporter assay, the transcription factor LSF was identified as a positive regulator of DPYD.

    Sequence Similarities: Belongs to the dihydropyrimidine dehydrogenase family.

    Molecular Weight

    11 kDa

    UniProt

    Q12882

    Pathways

    Ribonucleoside Biosynthetic Process
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