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Cytochrome P450 4F2 antibody [N2C2], Internal

GTX102722
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetCYP4F2
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Overview

  • Supplier
    GeneTex
  • Product Name
    Cytochrome P450 4F2 antibody [N2C2], Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.28 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID8529
  • Target name
    CYP4F2
  • Target description
    cytochrome P450 family 4 subfamily F member 2
  • Target synonyms
    CPF2, cytochrome P450 4F2, 20-HETE synthase, 20-hydroxyeicosatetraenoic acid synthase, CYPIVF2, arachidonic acid omega-hydroxylase, cytochrome P450, family 4, subfamily F, polypeptide 2, cytochrome P450, subfamily IVF, polypeptide 2, cytochrome P450-LTB-omega, docosahexaenoic acid omega-hydroxylase, leukotriene-B(4) 20-monooxygenase 1, leukotriene-B(4) omega-hydroxylase 1, phylloquinone omega-hydroxylase CYP4F2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP78329
  • Protein Name
    Cytochrome P450 4F2
  • Scientific Description
    This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. The enzyme starts the process of inactivating and degrading leukotriene B4, a potent mediator of inflammation. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F11, is approximately 16 kb away. [provided by RefSeq]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Podszun MC, Grebenstein N, Hofmann U, et al. High-dose supplementation with natural α-tocopherol does neither alter the pharmacodynamics of atorvastatin nor its phase I metabolism in guinea pigs. Toxicol Appl Pharmacol. 2013,266(3):452-8. doi: 10.1016/j.taap.2012.11.018
    Read this paper