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Last updated: 2016/12/4

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NSUN5 rabbit monoclonal antibody

  • Catalog # : H00055695-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human NSUN5 peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human NSUN5 is used for rabbit immunization.
    Customer or Abnova will decide on the preferred peptide sequence.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Purification:
  • Protein A
  • Isotype:
  • IgG
  • Quality Control Testing:
  • Antibody reactive against human NSUN5 peptide by ELISA and mammalian transfected lysate by Western Blot.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • 1. Customer may provide cell or tissue lysate for antibody screening.
    2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.
  • Library Construction:
  • Non-fusion antibody library from rabbit spleen (ARM Technology).
  • Expression:
  • Overexpression vector and transfection into 293H cell line.
  • Deliverable:
  • Up to three rabbit IgG clones of 1 mg each will be delivered to customer.
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Transfected lysate)
  • ELISA
  • Gene Information
  • GeneBank Accession#:
  • NSUN5
  • Gene Name:
  • NSUN5
  • Gene Alias:
  • FLJ10267,MGC986,NOL1,NOL1R,NSUN5A,WBSCR20,WBSCR20A,Ynl022cL,p120
  • Gene Description:
  • NOL1/NOP2/Sun domain family, member 5
  • Gene Summary:
  • This gene encodes a protein with similarity to p120 (NOL1), a 120-kDa proliferation-associated nucleolar antigen that is a member of an evolutionarily conserved protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq
  • Other Designations:
  • NOL1/NOP2/sun gene family member,Williams Beuren syndrome chromosome region 20A,Williams-Beuren syndrome critical region protein 20 copy A
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