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测量和解释点扩散函数,以确定共焦显微镜的分辨率并确保质量控制。

Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

机构信息

Wadsworth Center, New York State Department of Health, Albany, New York, USA.

出版信息

Nat Protoc. 2011 Nov 10;6(12):1929-41. doi: 10.1038/nprot.2011.407.

Abstract

This protocol outlines a procedure for collecting and analyzing point spread functions (PSFs). It describes how to prepare fluorescent microsphere samples, set up a confocal microscope to properly collect 3D confocal image data of the microspheres and perform PSF measurements. The analysis of the PSF is used to determine the resolution of the microscope and to identify any problems with the quality of the microscope's images. The PSF geometry is used as an indicator to identify problems with the objective lens, confocal laser scanning components and other relay optics. Identification of possible causes of PSF abnormalities and solutions to improve microscope performance are provided. The microsphere sample preparation requires 2-3 h plus an overnight drying period. The microscope setup requires 2 h (1 h for laser warm up), whereas collecting and analyzing the PSF images require an additional 2-3 h.

摘要

本方案概述了一种用于收集和分析点扩散函数(PSF)的方法。它描述了如何准备荧光微球样品,设置共焦显微镜以正确收集微球的 3D 共焦图像数据并进行 PSF 测量。PSF 的分析用于确定显微镜的分辨率,并确定显微镜图像质量的任何问题。PSF 几何形状用作指示,以识别物镜、共焦激光扫描组件和其他中继光学器件的问题。提供了识别 PSF 异常的可能原因和提高显微镜性能的解决方案。微球样品制备需要 2-3 小时,外加一个过夜干燥期。显微镜设置需要 2 小时(激光预热 1 小时),而收集和分析 PSF 图像则需要另外 2-3 小时。

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