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Application: Useful for the study of ARG2 enzymology, screening inhibitors, and selectivity profiling.
Background: Arginase enzymes convert arginine to ornithine through hydrolysis. Two known isoforms of Arginase exist, ARG1 and ARG2. This enzyme is involved in the regulation of a variety of immunological responses and is a major target in immunotherapy. ARG1/2 is overexpressed in myeloid-derived suppressor cells (MDSCs) and tumor-associated macrophages (TAMs). Overexpression of ARG1/2 results in depleted levels of arginine both intracellularly and extracellularly. As arginine levels are depleted in the microenvironment, immune cells are starved of this amino acid and the function of key immunological activators become impaired; T cell proliferation is inhibited, regulatory T cells become activated and inhibit CD4+ T cells, and immunosuppressants have increased longevity. Depleted arginine also results in the release of reactive nitrogen species and reactive oxygen species from TAMs and MDSCs. These reactive species cause T cell apoptosis and the activation and growth of antigen presenting cells.
Contraindications: DMSO > 1%, strong acids or bases, ionic detergents, high salt
Description: The ARG2 Inhibitor Screening Assay Kit is designed to measure ARG2 enzyme inhibition. The kit comes in a convenient format, with enough reaction solution and enzyme to perform a total of 400 reactions. The ARG2 Inhibitor Screening Assay Kit is simple to use. Inhibitor and enzyme are added to a sample containing thioarginine substrate. After a room temperature incubation, activity is determined by measuring the absorption of reaction product at λ=410-415 nm.
Storage Stability: Stable at least 6 months from date of receipt, when stored as directed. Kit components require different storage conditions. Be sure to store each component at the proper temperature upon arrival.
Warnings: Avoid freeze/thaw cycles.
Biosafety Level: Not applicable (BSL-1)
References: 1.Sedbrook, J.C., et al., PNAS. 1999 Feb; 96(3):1140-1145. 2.Woll, P.J., et al., PNAS. 1998 Mar; 85(6):1859-1863.
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