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Last updated: 2016/10/23
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CENPJ MaxPab rabbit polyclonal antibody (D01)MaxPab

  • Catalog # : H00055835-D01
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against a full-length human CENPJ protein.
  • Immunogen:
  • CENPJ (AAH24209.3, 1 a.a. ~ 372 a.a) full-length human protein.
  • Sequence:
  • Host:
  • Rabbit
  • 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.
  • Applications
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of CENPJ expression in transfected 293T cell line (H00055835-T01) by CENPJ MaxPab polyclonal antibody.

    Lane 1: CENPJ transfected lysate(43.2 KDa).
    Lane 2: Non-transfected lysate.
  • PDF DownloadProtocol Download
  • Immunoprecipitation
  • Immunoprecipitation
  • Immunoprecipitation of CENPJ transfected lysate using anti-CENPJ MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead (U0007), and immunoblotted with CENPJ purified MaxPab mouse polyclonal antibody (B01P) (H00055835-B01P).
  • PDF DownloadProtocol Download
  • Application Image
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Gene Information
  • Gene Name:
  • 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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