显微镜
反褶积
光学相干层析成像
断层摄影术
共焦显微镜
光学切片
光学
生物标本
荧光显微镜
薄层荧光显微镜
分辨率(逻辑)
光学层析成像
光学显微镜
投影(关系代数)
材料科学
扫描共焦电子显微镜
物理
计算机科学
人工智能
荧光
算法
扫描电子显微镜
作者
James Sharpe,Ulf Ahlgren,Paul Perry,Bill Hill,Allyson Ross,Jacob Hecksher‐Sørensen,Richard Baldock,Duncan Davidson
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2002-04-19
卷期号:296 (5567): 541-545
被引量:1166
标识
DOI:10.1126/science.1068206
摘要
Current techniques for three-dimensional (3D) optical microscopy (deconvolution, confocal microscopy, and optical coherence tomography) generate 3D data by “optically sectioning” the specimen. This places severe constraints on the maximum thickness of a specimen that can be imaged. We have developed a microscopy technique that uses optical projection tomography (OPT) to produce high-resolution 3D images of both fluorescent and nonfluorescent biological specimens with a thickness of up to 15 millimeters. OPT microscopy allows the rapid mapping of the tissue distribution of RNA and protein expression in intact embryos or organ systems and can therefore be instrumental in studies of developmental biology or gene function.
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