TPC2-A1-N is a powerful and Ca 2+ -permeable agonist of two pore channel 2 (TPC2) , which plays its role by mimicking the physiological actions of NAADP. TPC2-A1-P reproducibly evokes significant Ca 2+ responses from TPC2 ( EC 50 =7.8 μM ), and the effect can be blocked by several TPC blockers. TPC2-A1-N can be used to probe different functions of TPC2 channels in intact cells.
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