Dihydropyridine receptor (DHPR) and the sarcoplasmic reticulum ryanodine receptor (RyR) are two key components of the intracellular junctions, where depolarization of the surface membrane is converted into the release of Ca2+ from internal stores. Biochemicals that inhibit RyR-3 have many applications in biochemical and physiological research. Click on the product name to view detailed information such as the chemical structure and specific chemical properties for each of our RyR-3 Inhibitors. In stock RyR-3 Inhibitors are available for immediate shipping.
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