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Cyclic ADP-ribose ammonium (cADPR ammonium) is a potent calcium mobilization second messenger synthesized from NAD+ by ADP-ribosyl cyclase. It raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum and facilitates extracellular influx via TRPM2 channels [1][2][3].
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Description | Cyclic ADP-ribose ammonium (cADPR ammonium) is a potent calcium mobilization second messenger synthesized from NAD+ by ADP-ribosyl cyclase. It raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum and facilitates extracellular influx via TRPM2 channels [1][2][3]. |
In vitro | cADPR (20 nM) prompts a significant, rapid Ca2+ release in sea urchin egg homogenates [1]. cADPR (100 μM; 10 min) causes a sustained increase in intracellular calcium concentration in 64% of cultured astrocytes [4]. cADPR (100 μM) and heat (35-38.5 ℃) stimulate oxytocin OT release from isolated hypothalami of male mice in culture [5]. |
In vivo | cADPR (100 μM; push-pull type of brain microperfusion) elevats OT concentrations in ordinate or subordinate mice[5]. |
Relative Density. | no data available |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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