• Product nameAnti-XPB antibody
    See all XPB primary antibodies
  • Description
    Rabbit polyclonal to XPB
  • Tested applicationsSuitable for: WB, ICC/IFmore details
  • Species reactivity
    Reacts with: Mouse, Rat, Human
  • Immunogen

    Synthetic peptide:


    conjugated to KLH via an N-terminal added cysteine residue, corresponding to amino acids 765-782 of human XPB.



Our Abpromise guarantee covers the use of ab53198 in the following tested applications.

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

Application Abreviews Notes
  • Application notesICC/IF: Use at a concentration of 10 - 20 µg/ml.
    WB: Use at a concentration of 1 - 2 µg/ml. Detects a band of approximately 90 kDa (predicted molecular weight: 87 kDa).
    Diluting the antibody in PBS containing 1-3% non-fat dry milk and 0.05% TWEEN 20 is advised for WB.

    Not yet tested in other applications.
    Optimal dilutions/concentrations should be determined by the end user.
  • Target

    • FunctionATP-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.
    • Involvement in diseaseDefects 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.
    • Sequence similaritiesBelongs to the helicase family. RAD25/XPB subfamily.
      Contains 1 helicase ATP-binding domain.
      Contains 1 helicase C-terminal domain.
    • Cellular localizationNucleus.
    • Information by UniProt
    • Database links
    • Alternative names
      • 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

    References for Anti-XPB antibody (ab53198)

    ab53198 has not yet been referenced specifically in any publications.

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