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The data was published in the journal PLoS One in 2017. PMID: 29045486
The data was published in the journal PLoS One in 2017. PMID: 29045486
The data was published in the journal PLoS One in 2017. PMID: 29045486

Noxa antibody

GTX85521
GeneTex
TargetPmaip1
Product group Antibodies
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Overview

  • Supplier
    GeneTex
  • Product Name
    Noxa antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.5 - 2 microg/mL. IHC-P: 1 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Concentration
    1 mg/ml
  • Formulation
    Liquid
  • Gene ID58801
  • Target name
    Pmaip1
  • Target description
    phorbol-12-myristate-13-acetate-induced protein 1
  • Target synonyms
    N; Noxa; phorbol-12-myristate-13-acetate-induced protein 1; protein Noxa
  • Protein IDQ9JM54
  • Protein Name
    Phorbol-12-myristate-13-acetate-induced protein 1
  • Scientific Description
    Apoptosis is related to many diseases and development. The p53 tumor-suppressor protein induces apoptosis through transcriptional activation of several genes including p53R2, p53AIP1, and PUMA. A new p53 target gene, Noxa, was recently identified , which encodes a protein belonging to the subfamily of BH3-only proapoptic proteins. Noxa and PUMA are both transcriptional targets of p53 and BH3-only proteins. X-ray irradiation increased p53-dependent Noxa mRNA and protein levels. Noxa, when ectopically expressed, interacted with anti-apoptotic Bcl-2 family members, resulting in the activation of caspase-9 . Noxa, like PUMA, localized to mitochondria and induces apoptosis in response to p53 (1-3). Noxa and PUMA may represent direct mediators of p53-induced apoptosis. Increased levels of p53 and its target gene Noxa was found in the impaired tumor development (4).
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Thiamine deficiency activates hypoxia inducible factor-1alpha to facilitate pro-apoptotic responses in mouse primary astrocytes. Zera K et al., 2017, PLoS One
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