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Immunohistochemistry of Apaf1 in human skin tissue with Apaf1 (CT) antibody (GTX22000) at 20 microg/ml.
Immunohistochemistry of Apaf1 in human skin tissue with Apaf1 (CT) antibody (GTX22000) at 20 microg/ml.
Immunohistochemistry of Apaf1 in human skin tissue with Apaf1 (CT) antibody (GTX22000) at 20 microg/ml.

APAF1 antibody

GTX22000
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetAPAF1
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Overview

  • Supplier
    GeneTex
  • Product Name
    APAF1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1-10microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID317
  • Target name
    APAF1
  • Target description
    apoptotic peptidase activating factor 1
  • Target synonyms
    APAF-1; apoptotic protease-activating factor 1; CED4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO14727
  • Protein Name
    Apoptotic protease-activating factor 1
  • Scientific Description
    This gene encodes a cytoplasmic protein that initiates apoptosis. This protein contains several copies of the WD-40 domain, a caspase recruitment domain (CARD), and an ATPase domain (NB-ARC). Upon binding cytochrome c and dATP, this protein forms an oligomeric apoptosome. The apoptosome binds and cleaves caspase 9 preproprotein, releasing its mature, activated form. Activated caspase 9 stimulates the subsequent caspase cascade that commits the cell to apoptosis. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Metformin triggers the intrinsic apoptotic response in human AGS gastric adenocarcinoma cells by activating AMPK and suppressing mTOR/AKT signaling. Lu CC et al., 2019 Apr, Int J Oncol
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