首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >Validation of a competitive enzyme-linked immunosorbent assay for measuring the insulin-regulatable glucose transporter.
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Validation of a competitive enzyme-linked immunosorbent assay for measuring the insulin-regulatable glucose transporter.

机译:竞争性酶联免疫吸附测定法用于测量胰岛素调节性葡萄糖转运蛋白的验证。

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摘要

A novel competitive enzyme-linked immunosorbent assay (ELISA) for measuring the insulin-regulatable glucose transporter (GLUT4) has been developed in our laboratory. The purpose of the present study was to verify the competitive ELISA assay. Towards this goal, a time-course study was conducted in control Wistar rat hearts to determine the points at which insulin stimulated an initial and a maximal GLUT4 translocation. Plasma and intracellular membrane fractions were purified from heart ventricles isolated from rats either in the basal state or injected with insulin. GLUT4 content in the membrane fractions was quantified with both the competitive ELISA method and also with enhanced chemiluminescence (ECL) Western blot. It was shown that after insulin injection plasma membrane GLUT4 level increased about 60% at 15 min and intracellular GLUT4 decreased about 40-50% at 5 min and remained at this level throughout the remaining 25 min by both methods. In conclusion, the data from this study demonstrate that the ELISA assay is reliable as verified by the Western blot method.
机译:在我们的实验室中已经开发出一种新型的竞争性酶联免疫吸附测定(ELISA),用于测量胰岛素调节性葡萄糖转运蛋白(GLUT4)。本研究的目的是验证竞争性ELISA分析。为了实现这一目标,在对照Wistar大鼠心脏中进行了时程研究,以确定胰岛素刺激了初始和最大GLUT4易位的点。从基础状态或注射胰岛素的大鼠心室中纯化血浆和细胞内膜部分。膜部分中的GLUT4含量通过竞争性ELISA方法和增强的化学发光(ECL)Western印迹法进行定量。结果表明,注射胰岛素后,血浆膜GLUT4水平在15分钟时升高约60%,而细胞内GLUT4在5分钟时降低约40-50%,并且在这25分钟中,两种方法均保持这一水平。总之,这项研究的数据表明,ELISA试剂盒是可靠的,如Western blot方法所证实。

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