Raising the speed limits for 4D fluorescence microscopy

被引：32

作者：

Hammond, AT ^{[1
]}

Glick, BS ^{[1
]}

机构：

[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA

来源：

TRAFFIC | 2000年 / 1卷 / 12期

关键词：

confocal microscopy; deconvolution microscopy; microscopy; optical sectioning; photobleaching; piezoelectric; projection; video;

D O I：

10.1034/j.1600-0854.2000.011203.x

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Three-dimensional time-lapse (4D) fluorescence microscopy is becoming a routine experimental tool. This article summarizes current technologies, and describes a new method for speeding image acquisition during 4D confocal microscopy.

引用

页码：935 / 940

页数：6

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