Promega

Pgp-Glo Assay System

Varenummer: V3591
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The Pgp-Glo Assay Systems provide the necessary reagents for performing luminescent P-glycoprotein (Pgp) ATPase assays. Pgp, also known as MDR1 and ABCB1, is a 170kDa integral plasma membrane protein that functions as an ATP-dependent drug efflux pump and plays an important role in multidrug resistance and certain adverse drug-drug interactions. Compounds that interact with Pgp can be identified as stimulators or inhibitors of its ATPase activity. Compounds that are substrates for transport by Pgp typically stimulate its ATPase activity. The Pgp-Glo Assay detects the effects of compounds on recombinant human Pgp in a cell membrane fraction. The assay relies on the ATP dependence of the light-generating reaction of firefly luciferase. ATP is first incubated with Pgp; then the Pgp ATPase reaction is stopped, and the remaining unmetabolized ATP is detected as a luciferase-generated luminescent signal. Pgp-dependent decreases in luminescence reflect ATP consumption by Pgp; thus the greater the decrease in signal, the higher the Pgp activity. Accordingly, samples containing compounds that stimulate the Pgp ATPase will have significantly lower signals than untreated samples.|
Complete System: Cat.# V3591 includes all the reagents required to run the assay except the P-glycoprotein: A Pgp reaction buffer, MgATP, Verapamil, Na3VO4, and a lyophilized ATP detection reagent and its reconstitution buffer. Cat.# V3601 includes all the reagents provided in the Pgp-Glo™ System with the addition of Recombinant Human Pgp Membranes to provide a completely optimized kit.Stable Activities: "Glow-type" signal allows processing of multiple samples without concern of variability over time.Low False-Positive Rate: Use of a proprietary stabilized firefly luciferase and a proprietary luciferase assay formulation minimizes the incidence of false positives due to inhibition of luciferase by analytes when screening for compounds that affect Pgp activity.Simple: The simple protocol makes the assay amenable to high-throughput screening in multiwell plates.

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Christine Rindal Ibra 944 34 009 christine.rindal.ibra@nmas.no
Claudia Emmanuel 951 51 950 claudia.emmanuel@nmas.no
Monica Laukas 404 40 960 monica.laukas@nmas.no

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