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ELISA测定血清半胱氨酸蛋白酶抑制剂C
引用本文:单桂芬,林伟,荣墨克,张静春. ELISA测定血清半胱氨酸蛋白酶抑制剂C[J]. 中国实验诊断学, 2010, 14(1): 105-106
作者姓名:单桂芬  林伟  荣墨克  张静春
作者单位:1. 吉林大学第二医院,检验科,吉林,长春130041
2. 吉林大学中日联谊医院
摘    要:
目的建立ELISA方法测定血清半胱氨酸蛋白酶抑制剂C。方法以双抗体夹心ELISA方法测定血清半胱氨酸蛋白酶抑制剂C。结果该方法的线性范围可达100mg/L。参考值范围为:男,1.81±0.73mg/L。女,1.72±0.69mg/L。回收率为:99.1±3.1%。批内和批间分别为:5.8±0.5%、7.3±O.7%。结论该方法操作简便,快速,准确,适于临床常规应用。

关 键 词:ELISA方法  半胱氨酸蛋白酶抑制剂C  肾功能

The Method for Determination of Cystatin C by ELISA
SHAN Gui-fen,LIN Wei,RONG Mo-ke,et al.. The Method for Determination of Cystatin C by ELISA[J]. Chinese Journal of Laboratory Diagnosis, 2010, 14(1): 105-106
Authors:SHAN Gui-fen  LIN Wei  RONG Mo-ke  et al.
Affiliation:SHAN Gui-fen,LIN Wei,RONG Mo-ke,et al.(The Second Hospital of JiLin University,Changchun 130041,China)
Abstract:
Objective Th a enzyme-linked inununoserbent assay (ELISA) for measuring eystatin C. Methods e7 ystatin C in serum was measured by sandwieh-type ELISA. Results The linearity of method for up to 100 mg/L. The reference value range was: males, 1.81 ±0.73 mg/L. females, 1.72± 0.69 mg/L. The analytieal recovery was 99.1 ±3.1%. The mean eoeffieients of variation were 5.8±0.5% within-assay and 7.3±0.7% between-assay,respectively. Conclusion The method was simple,rapid and aeeu- rate to operate. It is suitable for routine elinieal labtatory use.
Keywords:ELISA  Cystatin C  kidney function  
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