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The culture medium was removed, and cells were loaded with 10 nM [H]taurine in Krebs-Ringer-HEPES buffer (KHB: 120 mM NaCl, 3 mM KCl, 2 mM CaCl, 2 mM MgCl, 20 mM glucose, 10 mM HEPES, pH 7.3) for 20 min at 37 C

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