Anti-XPB抗体[2327C4a] (ab70596)


  • 产品名称Anti-XPB抗体[2327C4a]
    参阅全部 XPB 一抗
  • 描述
    小鼠单克隆抗体[2327C4a] to XPB
  • 经测试应用适用于: WB, Dot blotmore details
  • 种属反应性
    与反应: Human
  • 免疫原

    Recombinant fragment (Human) from an N terminal region of XPB.

  • 阳性对照
    • Recombinant XPB protein.



Our Abpromise guarantee covers the use of ab70596 in the following tested applications.

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

应用 Ab评论 说明
WB Use at an assay dependent dilution. Predicted molecular weight: 87 kDa.
Dot blot Use at an assay dependent dilution.


  • 功能ATP-dependent 3'-5' DNA helicase, component of the core-TFIIH basal transcription factor, involved in nucleotide excision repair (NER) of DNA and, when complexed to CAK, in RNA transcription by RNA polymerase II. Acts by opening DNA either around the RNA transcription start site or the DNA damage.
  • 疾病相关Defects in ERCC3 are the cause of xeroderma pigmentosum complementation group B (XP-B) [MIM:610651]; also known as xeroderma pigmentosum II (XP2) or XP group B (XPB) or xeroderma pigmentosum group B combined with Cockayne syndrome (XP-B/CS). Xeroderma pigmentosum is an autosomal recessive pigmentary skin disorder characterized by solar hypersensitivity of the skin, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities. Some XP-B patients present features of Cockayne syndrome, including dwarfism, sensorineural deafness, microcephaly, mental retardation, pigmentary retinopathy, ataxia, decreased nerve conduction velocities.
    Defects in ERCC3 are a cause of trichothiodystrophy photosensitive (TTDP) [MIM:601675]. TTDP is an autosomal recessive disease characterized by sulfur-deficient brittle hair and nails, ichthyosis, mental retardation, impaired sexual development, abnormal facies and cutaneous photosensitivity correlated with a nucleotide excision repair (NER) defect. Neonates with trichothiodystrophy and ichthyosis are usually born with a collodion membrane. The severity of the ichthyosis after the membrane is shed is variable, ranging from a mild to severe lamellar ichthyotic phenotype. There are no reports of skin cancer associated with TTDP.
  • 序列相似性Belongs to the helicase family. RAD25/XPB subfamily.
    Contains 1 helicase ATP-binding domain.
    Contains 1 helicase C-terminal domain.
  • 细胞定位Nucleus.
  • Information by UniProt
  • 数据库链接
  • 别名
    • Basic transcription factor 2 89 kDa subunit antibody
    • BTF 2 antibody
    • BTF2 antibody
    • BTF2 p89 antibody
    • DNA excision repair protein ERCC-3 antibody
    • DNA repair protein complementing XP-B cells antibody
    • ERCC 3 antibody
    • ercc3 antibody
    • ERCC3_HUMAN antibody
    • Excision Repair Cross-complementing Rodent Repair deficiency complementation Group 3 antibody
    • GTF2H antibody
    • RAD 25 antibody
    • RAD25 antibody
    • TFIIH 89 kDa subunit antibody
    • TFIIH antibody
    • TFIIH basal transcription factor complex 89 kDa subunit antibody
    • TFIIH basal transcription factor complex helicase XPB subunit antibody
    • TFIIH p89 antibody
    • Xeroderma pigmentosum group B-complementing protein antibody
    see all

Anti-XPB antibody [2327C4a] 图像

Anti-XPB antibody [2327C4a] (ab70596)参考文献

ab70596 has not yet been referenced specifically in any publications.

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