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DDB2 (D4C4) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • 5416
  • USA
  • 2025年10月16日
  • W
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      DDB2 (D4C4) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to amino acids surrounding Ala174 of human DDB2

    • 应用范围

      W

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk

    • 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
    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) Endogenous 43 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    DDB2 (D4C4) Rabbit mAb detects endogenous levels of total DDB2 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to amino acids surrounding Ala174 of human DDB2.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Raji and HL-60 cells using DDB2 (D4C4) Rabbit mAb.

    Background

    D amaged D NA-B inding Protein (DDB) consists of a 127 kDa subunit (DDB-1) and a 48 kDa subunit (DDB-2) that contribute to the formation of the UV-damaged DNA-binding protein complex (UV-DDB) (1-3). In conjunction with CUL4A and ROC-1, the UV-DDB complex forms an E3 ubiquitin ligase that recognizes a broad spectrum of DNA lesions such as cyclobutane pyrimidine dimers, 6-4 photoproducts, apurinic sites and short mismatches. The complex polyubiquitinates components of the nucleotide excision repair pathway (4-6). Loss of DDB activity has been identified in a subset of xeroderma pigmentosum complementation group E (XP-E) patients and has been linked to the deficient repair of cyclobutane pyrimidine dimers in cells derived from these patients (7-10).

    1. Reardon, J.T. et al. (1993) J Biol Chem 268, 21301-8.
    2. Keeney, S. et al. (1993) J Biol Chem 268, 21293-300.
    3. Hwang, B.J. and Chu, G. (1993) Biochemistry 32, 1657-66.
    4. Chu, G. and Chang, E. (1990) Proc Natl Acad Sci USA 87, 3324-7.
    5. Hirschfeld, S. et al. (1990) Mol Cell Biol 10, 2041-8.
    6. Payne, A. and Chu, G. (1994) Mutat Res 310, 89-102.
    7. Chu, G. and Chang, E. (1988) Science 242, 564-7.
    8. Nichols, A.F. et al. (1996) J Biol Chem 271, 24317-20.
    9. Kataoka, H. and Fujiwara, Y. (1991) Biochem Biophys Res Commun 175, 1139-43.
    10. Keeney, S. et al. (1992) Mutat Res 273, 49-56.
    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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    图标文献和实验
    相关实验
    • Methods for the Detection of D-Amino-Acid Oxidase

      then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated

    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      组织化学分析。(图 C)使用Anti-Erk1/2 Mouse mAb 鼠单抗进行目的蛋白检测;(图 D) 使用p44/42 MAPK (Erk1/2)Rabbit mAb 兔单抗进行目的蛋白检测。 图 7 免疫组化实验检测Akt表达 注:使用 Anti-Akt (pan) Rabbit mAb 对正常小鼠肝组织进行免疫组织化学分析。(图 E)使用免疫组化试剂盒 M&R HRP/DAB Detection IHC Kit,抗体1:100 稀释;(图F)使用另一种试剂盒,抗体 1:100 稀释。

    • Methods for the Detection of D-Amino-Acid Oxidase

      min then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane

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