Serban I, Gavendo S, Modan M
J Lab Clin Med. 1977 May;89(5):1112-9.
A RIA method for the measurement of RRA is described, based upon the incubation of two dilutions of kidney extract with a fixed amount of EDTA-anticoagulated anephric rat plasma. The RIA of the generated angiotensin I is carried out with the commercially available NEN Kit. Recovery of angiotensin I added to the incubation mixture was 98 percent. There were 113 kidneys with a wide range of renin activity (52 to 1,274 ng. angiotensinl/mg. of kidney per hour) assayed. The within-assay coefficient of variation was uniform throughout the range, equalling 4.4 percent. The between-assay variance was practically identical with the within-assay variance. The confidence interval to the mean RRA level of one pair of readings was 5.4 percent of this mean.
本文描述了一种测量肾素反应活性(RRA)的放射免疫分析(RIA)方法,该方法基于将两份肾提取物稀释液与固定量的乙二胺四乙酸(EDTA)抗凝的无肾大鼠血浆进行孵育。生成的血管紧张素I的放射免疫分析使用市售的新英格兰核公司(NEN)试剂盒进行。添加到孵育混合物中的血管紧张素I的回收率为98%。共检测了113个肾脏,其肾素活性范围很广(每小时每毫克肾脏产生52至1274纳克血管紧张素I)。分析内变异系数在整个范围内是一致的,为4.4%。分析间方差与分析内方差几乎相同。一对读数的平均RRA水平的置信区间为此平均值的5.4%。