Characterization of sectioning fluorescence microscopy with thin uniform fluorescent layers: Sectioned Imaging Property or SIPcharts

被引:28
作者
Brakenhoff, GJ
Wurpel, GWH
Jalink, K
Oomen, L
Brocks, L
Zwier, JM
机构
[1] Univ Amsterdam, Swammerdam Inst Life Sci, Sect Mol Cytol, NL-1098 SM Amsterdam, Netherlands
[2] Univ Amsterdam, Ctr Adv Microscopy, NL-1098 SM Amsterdam, Netherlands
[3] Netherlands Canc Inst, Div Cell Biol, NL-1066 CX Amsterdam, Netherlands
关键词
3D microscopy; confocal microscopy; fluorescence microscopy; fluorescence photobleaching; image correction; multiphoton microscopy; sectioned imaging; sectioning microscopy; SIPcharts; two-photon microscopy;
D O I
10.1111/j.1365-2818.2005.01504.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
Thin, uniformly fluorescing reference layers can be used to characterize the imaging conditions in confocal, or more general, sectioning microscopy. Through-focus datasets of such layers obtained by standard microscope routines provide the basis for the approach. A set of parameters derived from these datasets is developed for defining a number of relevant sectioned imaging properties. The main characteristics of a particular imaging situation can then be summarized in a Sectioned Imaging Property-chart or SIPchart. We propose the use of such charts for the characterization of imaging properties in confocal and multiphoton microscopy. As such, they can be the basis for comparison of sectioned imaging condition characteristics, quality control, maintenance or reproduction of sectioned imaging conditions and other applications. Such charts could prove useful in documenting the more relevant properties of the instrumentation used in microscopy studies. The method carries the potential to provide the basis for a general characterization of sectioned imaging conditions as the layers employed can be characterized and fabricated to standard specifications. A limited number of such thin, uniformly fluorescing layers is available from our group for this purpose. Extension of the method to multiphoton microscopy is discussed.
引用
收藏
页码:122 / 132
页数:11
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