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Published on: May 30, 2016
Single objective light-sheet microscopy for high-speed whole-cell 3D super-resolution
Marjolein B M Meddens1, Sheng Liu2, Patrick S Finnegan3
1Department of Physics and Astronomy, University of New Mexico, 1919 Lomas Blvd NE, Albuquerque, NM 87131, USA; Department of Pathology, University of New Mexico, 2325 Camino de Salud, Albuquerque, NM 87131, USA.
Abstract:
We have developed a method for performing light-sheet microscopy with a single high numerical aperture lens by integrating reflective side walls into a microfluidic chip. These 45° side walls generate light-sheet illumination by reflecting a vertical light-sheet into the focal plane of the objective. Light-sheet illumination of cells loaded in the channels increases image quality in diffraction limited imaging via reduction of out-of-focus background light. Single molecule super-resolution is also improved by the decreased background resulting in better localization precision and decreased photo-bleaching, leading to more accepted localizations overall and higher quality images. Moreover, 2D and 3D single molecule super-resolution data can be acquired faster by taking advantage of the increased illumination intensities as compared to wide field, in the focused light-sheet.
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