Ploem J S
Appl Opt. 1987 Aug 15;26(16):3226-31. doi: 10.1364/AO.26.003226.
Fluorescence laser scanning microscopy (LSM) offers many advantages over conventional fluorescence microscopy. Very strong excitation light can be concentrated on small spots (0.5 microm) of the specimen, enabling the detection of low concentrations of fluorescent substances. The low levels of autofluorescence generated in the microscope objective and in the immersion oil in LSM provide images of great contrast, even with weakly fluorescent specimens. Confocal LSM permits the visualization of multiple focal layers of thespecimen and 3-D image reconstructions. Combination of images stored in computer memory allow the comparison of phase contrast and fluorescence images of the same area of the specimen enabling multiparameter analysis of cells.
荧光激光扫描显微镜(LSM)与传统荧光显微镜相比具有许多优势。非常强的激发光可以集中在标本的小点(0.5微米)上,从而能够检测低浓度的荧光物质。LSM中显微镜物镜和浸油产生的自发荧光水平很低,即使对于弱荧光标本也能提供高对比度的图像。共聚焦LSM可以使标本的多个焦层可视化并进行三维图像重建。存储在计算机内存中的图像组合允许比较标本同一区域的相差图像和荧光图像,从而实现细胞的多参数分析。