A mixture of primary vascular eicosanoids
Features
  • Each vial contains a mixture of standards packaged in amber ampules purged with argon
  • >1 ml provided at the concentration specified in the insert
  • Designed for direct snap and inject use in mass spectrometry applications
  • Ideally suited for method development and as a system suitability standard
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Primary Vascular Eicosanoid MaxSpec® LC-MS Mixture

Item No. 19667

Technical Information
Formulation
A solution in ethanol (1 μg/ml each compound)
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    This mixture contains a collection of vasoactive eicosanoids, including the characteristic metabolites of both prostaglandin I2 (PGI2; Item No. 18220) and thromboxane A2 (TXA2), as well as several additional HETE and EET metabolites produced by platelets and the cytochrome P450 pathway of arachidonic acid metabolism. The mixture is supplied in an amber ampule in which the headspace has been purged with argon to prevent lipid oxidation. This product has been designed for direct use in LC-MS applications. The solution may be serially diluted for preparation of calibrators and QC standards and/or used directly as a system suitability standard or tuning standard. After opening, we recommend that the mixture be transferred immediately to a 1 ml glass screw cap vial, to prevent solvent evaporation, and stored at -20°C. The mixture should be discarded after multiple freeze/thaw cycles.

    Whereas PGI2 is a potent vasodilator and inhibitor of human platelet aggregation, TXA2 causes irreversible platelet aggregation and contraction of vascular and bronchial smooth muscle. Because both are rapidly hydrolyzed and metabolized, TXB2 (Item No. 19030), 11-dehydro TXB2 (Item No. 19500), and 6-keto PGF (Item No. 15210) serve as useful markers for their synthesis.1,2 Certain HETEs and EETs have been shown to either inhibit platelet activation or regulate vasoconstriction.3,4,5,6,7,8,9

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ciabattoni, G., Pugliese, F., Davi, G., et alFractional conversion of thromboxane B2 to urinary 11-dehydrothromboxane B2 in man. Biochim. Biophys. Acta 992(1), 66-70 (1989).

    2. Brash, A.R., Jackson, E.K., Saggese, C.A., et alMetabolic disposition of prostacyclin in humans. J. Pharmacol. Exp. Ther. 226(1), 78-87 (1983).

    3. Hamberg, M., and Samuelsson, B. Prostaglandin endoperoxides. Novel transformations of arachidonic acid in human platelets. Proc. Natl. Acad. Sci. USA 71(9), 3400-3404 (1974).

    4. Diczfalusy, U., Falardeau, P., and Hammarström, S. Conversion of prostaglandin endoperoxides to C17-hydroxy acids catalyzed by human platelet thromboxane synthase. FEBS Lett. 84, 271-274 (1977).

    5. Ikei, K.N., Yeung, J., Apopa, P.L., et alInvestigations of human platelet-type 12-lipoxygenase: Role of lipoxygenase products in platelet activation. J. Lipid Res. 53(12), 2546-2559 (2012).

    6. McGiff, J.C., and Quilley, J. 20-HETE and the kidney: Resolution of old problems and new beginnings. Am. J. Physiol. 277(3), R607-R623 (1999).

    7. Katoh, T., Takahashi, K., Capdevila, J., et alGlomerular stereospecific synthesis and hemodynamic actions of 8,9-epoxyeicosatrienoic acid in rat kidney. Am. J. Physiol. 261(4 Pt 2), F578-F586 (1991).

    8. Graber, M.N., Alfonso, A., and Gill, D.L. Recovery of Ca2+ pools and growth in Ca2+ pool-depleted cells is mediated by specific epoxyeicosatrienoic acids derived from arachidonic acid. The Journal of Biological Chemisty 272(47), 29546-29553 (1997).

    9. Catella, F., Lawson, J.A., Fitzgerald, D.J., et alEndogenous biosynthesis of arachidonic acid epoxides in humans: Increased formation in pregnancy-induced hypertension. Proc. Natl. Acad. Sci. USA 87(15), 5893-5897 (1990).