CENPJ 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00055835-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

CENPJ transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: CENPJ transfected lysate ( 43.2 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-CENPJ full-length

    Host

    Human

    Theoretical MW (kDa)

    43.2

    Interspecies Antigen Sequence

    Mouse (83); Rat (81)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-CENPJ antibody (H00055835-B01) by Western Blots.

    SDS-PAGE Gel

    CENPJ transfected lysate.

    Western Blot

    Lane 1: CENPJ transfected lysate ( 43.2 KDa)
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — CENPJ

    Entrez GeneID

    55835

    GeneBank Accession#

    BC024209.2

    Protein Accession#

    -

    Gene Name

    CENPJ

    Gene Alias

    BM032, CPAP, LAP, LIP1, MCPH6, MGC131581, MGC131582, MGC142222, MGC142224

    Gene Description

    centromere protein J

    Omim ID

    608393 609279

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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