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This mixture contains several lipoxins and their precursor, arachidonic acid (Item No. 90010). 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 -80°C. The mixture should be discarded after multiple freeze/thaw cycles.
The fatty acids in this mixture represent the metabolic cascade of the lipoxins, a family of lipid mediators that are generated at the site of vascular and mucosal inflammation where they down-regulate polymorphonuclear leukocyte recruitment and function.1,2,3,4 Lipoxins are produced by human leukocytes via the oxygenation of arachidonic acid by either 15- or 5-lipoxygenase, which forms 15-HETE or 5-HETE intermediates before subsequent metabolism to lipoxin A4 (Item No. 90410) and B4 (Item No. 90420).1,5,6 15(R)-Lipoxin A4 (Item No. 90415) is derived from the aspirin-triggered formation of 15(R)-HETE (Item No. 34710) from arachidonic acid.7,8
WARNING This product is not for human or veterinary use.
1. Lipoxins: Novel series of biologically active compounds formed from arachidonic acid in human leukocytes. Proc. Natl. Acad. Sci. USA 81(17), 5335-5339 (1984).
2. Lipoxin A-
3. Lipoxin A4 and B4 are potent stimuli for human monocyte migration and adhesion: Selective inactivation by dehydrogenation and reduction. J. Exp. Med. 183(1), 137-146 (1996).
4. Lipoxin A4 and B4 inhibit leukotriene-
5. Lipoxin A. Stereochemistry and biosynthesis. The Journal of Biological Chemisty 261(35), 16340-16345 (1986).
6. On the stereochemistry and biosynthesis of lipoxin B. Proc. Natl. Acad. Sci. USA 83(7), 1983-1987 (1986).
7. Aspirin-
8. Aspirin triggers previously undescribed bioactive eicosanoids by human endothelial cell-