ArticleMicron (Oxford, England : 1993)2016
Simultaneous two color image capture for sub-diffraction localization fluorescence microscopy.
Article in Micron (Oxford, England : 1993), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Conventional fluorescence microscopy below the diffraction limit with simultaneous capture of two fluorophores in DNA origami.Proceedings of SPIE--the International Society for Optical Engineering · 2016Article
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2 authors.
Funding
Abstract
A sub-diffraction limit fluorescence localization microscope was constructed using a standard cooled 1.4 mega-pixel fluorescence charge-coupled device (CCD) camera to simultaneously resolve closely adjacent paired quantum dots on a flat surface with emissions of 540 and 630 nm. The images of the overlapping Airy discs were analyzed to determine the center of the point spread function after noise reduction using Fourier transformation analysis. The Cartesian coordinates of the centers of the point spread functions were compared in serial images. Histograms constructed from serial images fit well to Gaussian functions for resolving two quantum dots separated by as little as 10nm in the x-y coordinates. Statistical analysis of multiple pairs validated discrimination of inter-fluorophore distances that vary by 10nm. The method is simple and developed for x-y resolution of dilute fluorophores on a flat surface, not serial z sectioning.
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