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人胃蛋白酶原A和胃蛋白酶原C的放射免疫测定

Radioimmunoassay of human pepsinogen A and pepsinogen C.

作者信息

Biemond I, Jansen J B, Crobach L F, Kreuning J, Lamers C B

机构信息

Afdeling Maag-, Darm- en Leverziekten, Academisch Ziekenhuis, Leiden, The Netherlands.

出版信息

J Clin Chem Clin Biochem. 1989 Jan;27(1):19-25. doi: 10.1515/cclm.1989.27.1.19.

Abstract

We describe the development of radioimmunoassays to measure both human pepsinogen A and pepsinogen C concentrations in serum. The antibodies were raised in goats by immunization with purified pepsinogen A or C. The affinity constants of the respective antibodies were 20.10(10) l/mol and 7.10(10) l/mol. Pepsinogens A and C were labeled with Na 125I by the chloramine T method. The binding between labels and antibodies was inhibited by 0.50 at 0.82 ng pepsinogen A per tube and 2.1 ng pepsinogen C per tube. The detection limits of the assay of pepsinogen A and C were 0.12 microgram/l and 1.8 micrograms/l, respectively. Pepsinogen A and C were purified and added to a patient serum, showing a good recovery in the radioimmunoassays. Serial dilution of another patient serum, which contained a high concentration of both antigens, showed curves parallel to the standard curves. The intra- and interassay variations of these radioimmunoassays were evaluated. The intra-assay coefficients of variation for pepsinogen A were found to vary from 0.03 to 0.102 at concentrations in serum in the normal range, while the inter-assay coefficient of variation ranged from 0.118 to 0.194 at the same concentrations in serum. For the pepsinogen C radioimmunoassay we found intra-assay coefficients of variation between 0.126 and 0.147 at concentrations in serum in the normal range, while the inter-assay coefficient of variation ranged from 0.174 to 0.325 for the same sera. In 201 blood donors we found a mean serum concentration of pepsinogen A of 59 micrograms/l and a mean serum concentration of pepsinogen C of 15 micrograms/l. There was a significant relationship between these values (r = 0.779, p less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们描述了用于测量血清中人类胃蛋白酶原A和胃蛋白酶原C浓度的放射免疫分析方法的开发。通过用纯化的胃蛋白酶原A或C免疫山羊来制备抗体。各自抗体的亲和常数分别为20.10(10) l/mol和7.10(10) l/mol。采用氯胺T法用Na 125I标记胃蛋白酶原A和C。每管中0.82 ng胃蛋白酶原A和2.1 ng胃蛋白酶原C可抑制标记物与抗体之间的结合。胃蛋白酶原A和C检测限分别为0.12微克/升和1.8微克/升。胃蛋白酶原A和C经纯化后加入患者血清,在放射免疫分析中显示出良好的回收率。对另一份含有高浓度两种抗原的患者血清进行系列稀释,所得曲线与标准曲线平行。评估了这些放射免疫分析的批内和批间变异。发现在血清浓度处于正常范围时,胃蛋白酶原A的批内变异系数在0.03至0.102之间,而相同血清浓度下批间变异系数在0.118至0.194之间。对于胃蛋白酶原C放射免疫分析,我们发现在血清浓度处于正常范围时,批内变异系数在0.126至0.147之间,而相同血清的批间变异系数在0.174至0.325之间。在201名献血者中,我们发现胃蛋白酶原A的平均血清浓度为59微克/升,胃蛋白酶原C的平均血清浓度为15微克/升。这些值之间存在显著相关性(r = 0.779,p < 0.001)。(摘要截短至250字)

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