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WB analysis of extracts from COS-7 tissue using GTX55399 Bcr (phospho Tyr360) antibody. Left : Primary antibody Right : Primary antibody pre-incubated with the antigen specific peptide
WB analysis of extracts from COS-7 tissue using GTX55399 Bcr (phospho Tyr360) antibody. Left : Primary antibody Right : Primary antibody pre-incubated with the antigen specific peptide
WB analysis of extracts from COS-7 tissue using GTX55399 Bcr (phospho Tyr360) antibody. Left : Primary antibody Right : Primary antibody pre-incubated with the antigen specific peptide

Bcr (phospho Tyr360) antibody

GTX55399
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetBCR
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Overview

  • Supplier
    GeneTex
  • Product Name
    Bcr (phospho Tyr360) antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID613
  • Target name
    BCR
  • Target description
    BCR activator of RhoGEF and GTPase
  • Target synonyms
    ALL; BCR, RhoGEF and GTPase activating protein; BCR/FGFR1 chimera protein; BCR1; breakpoint cluster region; breakpoint cluster region protein; CML; D22S11; D22S662; FGFR1/BCR chimera protein; PHL; renal carcinoma antigen NY-REN-26
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP11274
  • Protein Name
    Breakpoint cluster region protein
  • Scientific Description
    A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac. Two transcript variants encoding different isoforms have been found for this gene. [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 BCR using anti-BCR antibody (A00022-2). 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 Jurkat whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human HEK293 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue 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-BCR antigen affinity purified polyclonal antibody (Catalog # A00022-2) at 0.25 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 BCR at approximately 160 kDa. The expected band size for BCR is at 160 kDa.
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