Schmolke M F, Guder W G, Horster M F
Enzyme. 1984;31(3):187-90. doi: 10.1159/000469522.
Microenzymatic methods have been utilized in the past to quantify the activity of Na-K-ATPase in tubular segments of the mammalian nephron. The assay reported here measures the precipitated inorganic phosphate liberated by the hydrolysis of gamma-32P-ATP. Activity data in single nephron segments of the cortical collecting tubule (CCT) confirm previous work; specifically, first data on enzyme activity in small cultured cell populations derived from CCT demonstrate that the Na-carrier enzyme can be quantified in nephron cell cultures.
过去曾使用微酶法来定量测定哺乳动物肾单位肾小管段中钠钾-ATP酶的活性。本文报道的测定方法测量由γ-32P-ATP水解释放的沉淀无机磷酸盐。皮质集合管(CCT)单个肾单位段的活性数据证实了先前的研究结果;具体而言,来自CCT的小培养细胞群体中酶活性的首批数据表明,钠载体酶可在肾单位细胞培养物中进行定量测定。