A quantum dot-based microfluidic multi-window platform for quantifying the biomarkers of breast cancer cells.

IF 1.4
Seyong Kwon, Minseok S Kim, Eun Sook Lee, Jang Sihn Sohn, Je-Kyun Park
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引用次数: 9

Abstract

Conventional molecular profiling methods using immunochemical assays have limits in terms of multiplexity and the quantification of biomarkers in investigation of cancer cells. In this paper, we demonstrate a quantum dot (QD)-based microfluidic multiple biomarker quantification (QD-MMBQ) method that enables labeling of more than eight proteins immunochemically on cell blocks within 1 h, in a quantitative manner. An internal reference, β-actin, was used as a loading control to compensate for differences in not only the cell number but also in staining quality among specimens. Furthermore, the microfluidic blocking method exhibited less nonspecific binding of QDs than the conventional static blocking method.

基于量子点的微流控多窗口平台用于定量乳腺癌细胞的生物标志物。
使用免疫化学分析的传统分子分析方法在研究癌细胞的生物标志物的多样性和定量方面存在局限性。在本文中,我们展示了一种基于量子点(QD)的微流体多重生物标志物定量(QD- mmbq)方法,该方法能够在1小时内对细胞块上的8种以上蛋白质进行免疫化学定量标记。内参β-肌动蛋白被用作上样对照,以补偿不同标本间细胞数量和染色质量的差异。此外,与传统的静态阻断方法相比,微流控阻断方法显示出更少的量子点非特异性结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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