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Myeloperoxidase Chlorination Assay Kit

Cat no: 10006438

Myeloperoxidase Chlorination Assay Kit

Cayman's Myeloperoxidase Chlorination Assay provides a convenient fluorescence-based method for detecting the MPO chlorination activity in both crude cell lysates and purified enzyme preparations. The assay utilizes the non-fluorescent 2-[6-(4-aminophenoxy)-3-oxo-3H-xanthen-9-yl]-benzoic acid (APF), which is selectively cleaved by hypochlorite (-OCl) to yield the highly fluorescent compound fluorescein. Fluorescein fluorescence is analyzed using an excitation wavelength between 480-490 nm and an emission wavelength between 515-520 nm. The kit includes an MPO-specific inhibitor for distinguishing MPO activity from MPO-independent fluroescence.

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SPECIFICATIONS

Catalog Number

10006438

Form

192 Well

P Type

Assay Kits

Weight

0

Storage Temp

4

Shipping Temp

4

Additional Info

Myeloperoxidase (MPO) is a member of the heme peroxidase superfamily and is stored within the azurophilic granules of leukocytes. MPO is found within circulating neutrophils, monocytes, and some tissue macrophages. A unique activity of MPO is its ability to use chloride as a cosubstrate with hydrogen peroxide (H2O2) to generate chlorinating oxidants such as hypochlorous acid, a potent antimicrobial agent. Recently, evidence has emerged that MPO-derived oxidants contribute to tissue damage and the initiation and propagation of acute and chronic vascular inflammatory diseases. The fact that circulating levels of MPO have been shown to predict risks for major adverse cardiac events and that levels of MPO-derived chlorinated compounds are specific biomarkers for disease progression, has attracted considerable interest in the development of therapeutically useful MPO inhibitors. MPO also oxidizes a variety of substrates, including phenols and anilines, via the classic peroxidation cycle. The relative concentrations of chloride and the reducing substrate determine whether MPO uses H2O2 for chlorination or peroxidation. Assays based on measurement of chlorination activity are more specific for MPO than those based on peroxidase substrates because peroxidases generally do not produce hypochlorous acid. The only exception is eosinophil peroxidase that produces hypochlorous acid at pH below 5. The chlorination activity of MPO has a neutral pH optimum, therefore the assay conditions can be set so that only MPO activity is specifically measured. Cayman

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