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活细胞中微管和肌动蛋白的荧光斑点显微镜检查(FSM)。

Fluorescent speckle microscopy (FSM) of microtubules and actin in living cells.

作者信息

Waterman-Storer Clare

机构信息

The Scripps Research Institute, La Jolla, California, USA.

出版信息

Curr Protoc Cell Biol. 2002 Feb;Chapter 4:Unit 4.10. doi: 10.1002/0471143030.cb0410s13.

Abstract

Fluorescent speckle microscopy (FSM), a combination of conventional wide-field fluorescent light microscopy and digital imaging with a low-noise, charge-coupled device (CCD) camera, has been developed to allow visualization of assembly/disassembly dynamics, movement, and turnover of macromolecule assemblies in vivo and in vitro. FSM uses a low level of fluorescent subunits to avoid high background. This produces an image of speckled molecules that co-assemble with endogenous molecules and are followed to characterize dynamic events in living cells.

摘要

荧光斑点显微镜术(FSM)是传统宽视野荧光显微镜与使用低噪声电荷耦合器件(CCD)相机的数字成像技术的结合,它已被开发用于在体内和体外观察大分子组装体的组装/拆卸动力学、运动和周转。FSM使用低水平的荧光亚基以避免高背景。这产生了与内源性分子共同组装的斑点分子图像,并通过追踪这些图像来表征活细胞中的动态事件。

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