Teresa S. Hawley, Robert G. Hawley, William G. Telford
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引用次数: 9
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Abstract
Fluorescent proteins have become standard tools for cell and molecular biologists. The color palette of fluorescent proteins spans the ultraviolet, visible, and near-infrared spectrum. Utility of fluorescent proteins has been greatly facilitated by the availability of compact and affordable solid state lasers capable of providing various excitation wavelengths. In theory, the plethora of fluorescent proteins and lasers make it easy to detect multiple fluorescent proteins simultaneously. However, in practice, heavy spectral overlap due to broad excitation and emission spectra presents a challenge. In conventional flow cytometry, careful selection of excitation wavelengths and detection filters is necessary. Spectral flow cytometry, an emerging methodology that is not confined by the “one color, one detector” paradigm, shows promise in the facile detection of multiple fluorescent proteins. This chapter provides a synopsis of fluorescent protein development, a list of commonly used fluorescent proteins, some practical considerations and strategies for detection, and examples of applications. © 2017 by John Wiley & Sons, Inc.
流式细胞术用荧光蛋白
荧光蛋白已经成为细胞和分子生物学家的标准工具。荧光蛋白的调色板横跨紫外线、可见光和近红外光谱。荧光蛋白的使用已经大大促进了紧凑和负担得起的固体激光器的可用性,能够提供各种激发波长。从理论上讲,大量的荧光蛋白和激光使得同时检测多种荧光蛋白变得容易。然而,在实际应用中,由于激发和发射光谱较宽,导致光谱重叠严重,这给光学系统带来了挑战。在传统的流式细胞术中,必须仔细选择激发波长和检测滤波器。光谱流式细胞术是一种新兴的方法,它不受“一种颜色,一种检测器”范式的限制,在多种荧光蛋白的简便检测中显示出前景。本章概述了荧光蛋白的发展,列出了常用的荧光蛋白,一些实际的注意事项和检测策略,以及应用实例。©2017 by John Wiley &儿子,Inc。
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