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HPLC method for determination of lipoxygenase positional specific products.

Journal of pharmaceutical and biomedical analysis (2013-06-26)
Peter Hoffman, Drahomíra Rauová, Lýdia Bezáková, Marek Obložinský, Peter Mikuš
ZUSAMMENFASSUNG

Mammalian lipoxygenases (LOXs) play an important role in physiological and pathological processes through the biosynthesis of lipid mediators-leukotrienes, lipoxins and other arachidonic acid derivatives.There are four major families of LOXs that can be analyzed through the production of hydroxyeicosatetraenoic acids (HETEs). No analytical method to detect 5-, 8-, 12- and 15-HETE in one run has been published to date. The HPLC method combines reversed-phase separative column Nucleosil 120-5 C18 and NP column Zorbax Rx.SIL for identification. This conjunction enables separation of 12-HETE and 15-HETE to the baseline which is essential in 12/15-LOX research and elution of all four HETEs in one run. The method was successfully tested on partially purified LOXs from rat lung cytosol.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Arachidonsäure, >95.0% (GC)
Sigma-Aldrich
Arachidonsäure, from non-animal source, ≥98.5% (GC)
Sigma-Aldrich
Lipoxidase Zubereitung aus Glycine max (soybean), Type I-B, lyophilized powder, ≥50,000 units/mg solid
Sigma-Aldrich
Lipoxidase Zubereitung aus Glycine max (soybean), Type V, ammonium sulfate suspension, 500,000-1,000,000 units/mg protein