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DcR1 antibody [TRAIL-R3-02] (Azide Free)

GTX79877
GeneTex
ApplicationsFlow Cytometry
Product group Antibodies
TargetTNFRSF10C
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Overview

  • Supplier
    GeneTex
  • Product Name
    DcR1 antibody [TRAIL-R3-02] (Azide Free)
  • Delivery Days Customer
    9
  • Applications
    Flow Cytometry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    TRAIL-R3-02
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID8794
  • Target name
    TNFRSF10C
  • Target description
    TNF receptor superfamily member 10c
  • Target synonyms
    antagonist decoy receptor for TRAIL/Apo-2L; CD263; cytotoxic TRAIL receptor-3; DCR1; DCR1-TNFR; decoy receptor 1; decoy TRAIL receptor without death domain; LIT; lymphocyte inhibitor of TRAIL; TNF-related apoptosis-inducing ligand receptor 3; TRAILR3; TRAIL-R3; TRID; tumor necrosis factor receptor superfamily member 10C; tumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDO14798
  • Protein Name
    Tumor necrosis factor receptor superfamily member 10C
  • Scientific Description
    The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

References

  • The Roles of ROS and Caspases in TRAIL-Induced Apoptosis and Necroptosis in Human Pancreatic Cancer Cells. Zhang M et al., 2015, PLoS One
    Read more

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