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单磁珠水平的名义有效免疫反应体积。

Nominal effective immunoreaction volume of magnetic beads at single bead level.

机构信息

College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058, China.

College of Life Information Science and Instrument Engineering, Hangzhou Dianzi University, Hangzhou 310018, China.

出版信息

J Zhejiang Univ Sci B. 2017;18(10):845-853. doi: 10.1631/jzus.B1600358.

Abstract

Immunomagnetic bead (IMB)-based enzyme-linked immunosorbent assay (ELISA) has been the tool frequently used for protein detection in research and clinical laboratories. For most ELISA reactions the recommended dosage of IMBs is usually according to their weight (mg) or mass fraction (w/v) instead of the bead number. Consequently, the processes occurring in the immediate vicinity of the IMBs have always been ignored by researchers and they cannot be revealed in detail during the ELISA reaction. In this paper, we established the relationship between number of IMBs and colorimetric results, and further proposed a new concept of "nominal effective immunoreaction volume (NEIV)" to characterize a single IMB during ELISA reaction. Results showed that the NEIV of a single IMB has a constant value, which is unrelated to the amount of beads and the concentration of antigen. Optimal results of the colorimetric ELISA are achieved when the incubation volume meets each IMB's NEIV and is no longer enhanced by increasing the incubation volume. Thus, the reliable and relatively precise number of IMBs for ELISA detection during practical application could be determined. Most importantly, a study using IMB's NEIV would lay the foundation for a kinetics analysis of IMBs and antigens for future study.

摘要

基于免疫磁珠(IMB)的酶联免疫吸附测定(ELISA)已成为研究和临床实验室中常用的蛋白质检测工具。对于大多数 ELISA 反应,IMB 的推荐剂量通常是根据其重量(mg)或质量分数(w/v)而不是珠数来确定的。因此,研究人员一直忽略了 IMB 附近发生的过程,并且无法在 ELISA 反应过程中详细揭示这些过程。在本文中,我们建立了 IMB 数量与比色结果之间的关系,并进一步提出了“标称有效免疫反应体积(NEIV)”的新概念,以表征 ELISA 反应过程中的单个 IMB。结果表明,单个 IMB 的 NEIV 具有恒定值,与珠数和抗原浓度无关。当孵育体积满足每个 IMB 的 NEIV 且不再通过增加孵育体积而增强时,比色 ELISA 可获得最佳结果。因此,可以确定实际应用中 ELISA 检测的可靠且相对精确的 IMB 数量。最重要的是,使用 IMB 的 NEIV 进行的研究将为未来的研究奠定 IMB 和抗原动力学分析的基础。

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