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Last updated: 2014/7/28
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ERCC8 MaxPab mouse polyclonal antibody (B02)MaxPab

  • Catalog # : H00001161-B02
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human ERCC8 protein.
  • Immunogen:
  • ERCC8 (NP_000073.1, 1 a.a. ~ 396 a.a) full-length human protein.
  • Sequence:
  • MLGFLSARQTGLEDPLRLRRAESTRRVLGLELNKDRDVERIHGGGINTLDIEPVEGRYMLSGGSDGVIVLYDLENSSRQSYYTCKAVCSIGRDHPDVHRYSVETVQWYPHDTGMFTSSSFDKTLKVWDTNTLQTADVFNFEETVYSHHMSPVSTKHCLVAVGTRGPKVQLCDLKSGSCSHILQGHRQEILAVSWSPRYDYILATASADSRVKLWDVRRASGCLITLDQHNGKKSQAVESANTAHNGKVNGLCFTSDGLHLLTVGTDNRMRLWNSSNGENTLVNYGKVCNNSKKGLKFTVSCGCSSEFVFVPYGSTIAVYTVYSGEQITMLKGHYKTVDCCVFQSNFQELYSGSRDCNILAWVPSLYEPVPDDDETTTKSQLNPAFEDAWSSSDEEG
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • No additive
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • For IHC and IF applications, antibody purification with Protein A will be needed prior to use.
  • Applications
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of ERCC8 expression in transfected 293T cell line (H00001161-T02) by ERCC8 MaxPab polyclonal antibody.

    Lane 1: ERCC8 transfected lysate(43.56 KDa).
    Lane 2: Non-transfected lysate.
  • Protocol Download
  • Detection Antibody
  • Application Image
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Detection Antibody
  • Gene Information
  • Entrez GeneID:
  • 1161
  • Gene Name:
  • ERCC8
  • Gene Alias:
  • CKN1,CSA
  • Gene Description:
  • excision repair cross-complementing rodent repair deficiency, complementation group 8
  • Gene Summary:
  • This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. [provided by RefSeq
  • Other Designations:
  • Cockayne syndrome WD-repeat protein CSA,DNA excision repair protein ERCC-8
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