DPYD (D35A8) Rabbit mAb

DPYD (D35A8) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月24日
  • W
  • H,M,R,Mk,Dg
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    • 详细信息
    • 技术资料
    • 抗体英文名

      DPYD (D35A8) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues near the amino terminus of human DPYD protein

    • 应用范围

      W

    • 保质期

      详见说明书

    • 适应物种

      H,M,R,Mk,Dg

    • 库存

      大量

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  Dg=Dog
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W H (M) (R) (Mk) (Dg) Endogenous 110 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    DPYD (D35A8) Rabbit mAb detects endogenous levels of total DPYD protein. The antibody also detects a 50-60 kDa band of unknown origin by western blot.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human DPYD protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa and IGROV-1 cells using DPYD (D35A8) Rabbit mAb.

    Background

    Dihydropyrimidine dehydrogenase (DPD, DPYD) catalyzes the initial and rate-limiting step in uracil and thymidine catabolism as well as catabolism of the chemotherapeutic drug 5-fluorouracil (5-FU) and its derivatives. DPYD deficiency, which results from mutations in the DPYD gene, causes errors in pyrimidine metabolism and potentially life-threatening side effects in cancer patients treated with 5-FU (reviewed in 1). As a result, ongoing work examines whether or how DPYD gene variation and protein expression can be used to predict 5-FU toxicity (1,2). Several genes that impart resistance to 5-FU were recently identified in human hepatocellular carcinoma (HCC). AEG-1, which is highly expressed in HCC, increases the expression of DPYD. DPYD is expressed more highly in HCC than in normal liver, and this is thought to be one mechanism of 5-FU resistance (3,4).

    1. Yen, J.L. and McLeod, H.L. (2007) Eur J Cancer 43, 1011-6.
    2. Ofverholm, A. et al. (2010) Clin Biochem 43, 331-4.
    3. Yoo, B.K. et al. (2009) Proc Natl Acad Sci U S A 106, 12938-43.
    4. Yoo, B.K. et al. (2009) J Clin Invest 119, 465-77.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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