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WB analysis of Jurkat cells using GTX45813 CENPB antibody at 0.2-1microg/ml.
WB analysis of Jurkat cells using GTX45813 CENPB antibody at 0.2-1microg/ml.
WB analysis of Jurkat cells using GTX45813 CENPB antibody at 0.2-1microg/ml.

CENPB antibody, C-term

GTX45813
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetCENPB
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Overview

  • Supplier
    GeneTex
  • Product Name
    CENPB antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.2-2.5 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID1059
  • Target name
    CENPB
  • Target description
    centromere protein B
  • Target synonyms
    CENP-B; centromere autoantigen B; centromere protein B, 80kDa; major centromere autoantigen B
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP07199
  • Protein Name
    Major centromere autoantigen B
  • Scientific Description
    This gene product is a highly conserved protein that facilitates centromere formation. It is a DNA-binding protein that is derived from transposases of the pogo DNA transposon family. It contains a helix-loop-helix DNA binding motif at the N-terminus, and a dimerization domain at the C-terminus. The DNA binding domain recognizes and binds a 17-bp sequence (CENP-B box) in the centromeric alpha satellite DNA. This protein is proposed to play an important role in the assembly of specific centromere structures in interphase nuclei and on mitotic chromosomes. It is also considered a major centromere autoantigen recognized by sera from patients with anti-centromere antibodies. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of CENPB using anti-CENPB antibody (A05140-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human HEK293 whole cell lysates, Lane 5: human MCF-7 whole cell lysates, Lane 6: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CENPB antigen affinity purified polyclonal antibody (Catalog # A05140-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CENPB at approximately 80 kDa. The expected band size for CENPB is at 80 kDa.
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