返回
Image scanning microscopy with a quadrant detector
DOI:10.1364/OL.40.005355.png)
摘要
En 中文
Confocal scanning microscopy (CSM) is the most widely used modern optical microscopy technique. Theoretically, it allows the diffraction barrier to be surpassed by a factor of root 2, but practically this improvement is sacrificed to obtain a good signal-to-noise ratio (SNR). Image scanning microscopy (ISM) solves this limitation but, in the current implementations, the system complexity is increased and the versatility of CSM is reduced. Here we show that ISM can be straightforwardly implemented by substituting the single point detector of a confocal microscope with a quadrant detector of the same size, thus using a small number of detector elements. This implementation offers resolution close to the CSM theoretical value and improves the SNR by a factor of 1.5 with respect to the CSM counterpart without losing the optical sectioning capability and the system versatility. (C) 2015 Optical Society of America
Keyword:
STRUCTURED ILLUMINATION MICROSCOPY
FLUORESCENCE MICROSCOPY
SUPER-RESOLUTION
SUPERRESOLUTION
LIMIT
LIVE
AI总结
对已上传原文的论文进行重点信息的提取,主要内容包括:简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。
期刊
IF:
3.3
论文数:
4.0W
被引数:
7.6W
机构
引用论文
Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination通过结构化照明在宽场荧光显微镜中提高三维分辨率
BIOPHYSICAL JOURNAL
IF3.1
Instant super-resolution imaging in live cells and embryos via analog image processing通过模拟图像处理在活细胞和胚胎中进行即时超分辨率成像
NATURE METHODS
IF32.1
Urinary uromodulin independently predicts end-stage renal disease and rapid kidney function decline in a cohort of chronic kidney disease patients
Medicine
IF0
Resolution doubling in live, multicellular organisms via multifocal structured illumination microscopy
NATURE METHODS
IF32.1

