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Last updated: 2017/3/19

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CENPJ rabbit monoclonal antibody

  • Catalog # : H00055835-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human CENPJ peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human CENPJ 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 CENPJ 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#:
  • CENPJ
  • Gene Name:
  • CENPJ
  • Gene Alias:
  • BM032,CPAP,LAP,LIP1,MCPH6,MGC131581,MGC131582,MGC142222,MGC142224
  • Gene Description:
  • centromere protein J
  • Gene Summary:
  • This gene encodes a protein that belongs to the centromere protein family. During cell division, this protein plays a structural role in the maintenance of centrosome integrity and normal spindle morphology, and it is involved in microtubule disassembly at the centrosome. This protein can function as a transcriptional coactivator in the Stat5 signaling pathway, and also as a coactivator of NF-kappaB-mediated transcription, likely via its interaction with the coactivator p300/CREB-binding protein. Mutations in this gene are associated with primary autosomal recessive microcephaly, a disorder characterized by severely reduced brain size and mental retardation. [provided by RefSeq
  • Other Designations:
  • LAG-3-associated protein,LYST-interacting protein LIP1,LYST-interacting protein LIP7,OTTHUMP00000018137,centrosomal P4.1-associated protein
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