Thread-paper, and fabric enzyme-linked immunosorbent assays (ELISA)

被引:13
作者
Gonzalez, Ariana [1 ]
Gaines, Michelle [1 ]
Gallegos, Laura Y. [1 ]
Guevara, Ricardo [1 ]
Gomez, Frank A. [1 ]
机构
[1] Calif State Univ Los Angeles, Dept Chem & Biochem, 5151 State Univ Dr, Los Angeles, CA 90032 USA
基金
美国国家科学基金会;
关键词
Enzyme-linked immunosorbent assays; Microfluidics thread/paper-based analytical device; Microfluidic fabric-based analytical device; Microfluidic thread-based analytical device; Microfluidics; LOW-COST; MICROFLUIDIC DEVICE; DOT-ELISA; PLATFORM; IMMUNOASSAY;
D O I
10.1016/j.ymeth.2018.02.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Enzyme-linked immunosorbent assay (ELISA) is an immunological assay commonly used to measure antibodies, antigens, proteins, and glycoproteins in biological samples. While the procedure is routine and straightforward, there are a number of variables (reagent selection, volume measurement, temperature, and time) that if not carefully considered, can affect the test outcome. Herein, we describe the development of microfluidic thread/paper-based analytical devices (mu TPAD), microfluidic fabric-based analytical devices (mu FAD), and microfluidic thread-based analytical devices (mu TAD) as new platforms for ELISA. The quantitative detection of biotinylated goat anti-mouse IgG (system one) and rabbit IgG (system two) antibodies via colorimetric analysis is detailed. We explain the design and fabrication of the devices and the step-by-step protocol for the ELISA. A comparison between the techniques is described and the results obtained from them elucidated. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
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