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ERCC6 (Human) Recombinant Protein (Q01)

  • Catalog # : H00002074-Q01
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Human ERCC6 partial ORF ( NP_000115, 1394 a.a. - 1493 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • RARNHLILPERLESESGHLQEASALLPTTEHDDLLVEMRNFIAFQAHTDGQASTREILQEFESKLSASQSCVFRELLRNLCTFHRTSGGEGIWKLKPEYC
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 36.74
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue.

    QC Testing of H00002074-Q01
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 2074
  • Gene Name:
  • ERCC6
  • Gene Alias:
  • ARMD5,CKN2,COFS,COFS1,CSB,RAD26
  • Gene Description:
  • excision repair cross-complementing rodent repair deficiency, complementation group 6
  • Gene Summary:
  • This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The protein has ATP-stimulated ATPase activity; there are contradictory publications reporting presence or absence of helicase activity. The protein appears to interact with several transcription and excision repair proteins, and may promote complex formation at repair sites. Mutations in this gene result in Cockayne syndrome type B. [provided by RefSeq
  • Other Designations:
  • Cockayne syndrome group B protein,OTTHUMP00000019581,Rad26 homolog
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