Imaging volumes as thick as whole cells at three-dimensional (3D) super-resolution is required to reveal unknown features of cellular organization. We report a light microscope that generates images with translationally invariant 30 x 30 x 75 nm resolution over a depth of several micrometers. This method, named biplane (BP) FPALM, combines a double-plane detection scheme with fluorescence photoactivation localization microscopy (FPALM) enabling 3D sub-diffraction resolution without compromising speed or sensitivity
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We demonstrate three-dimensional (3D) super-resolution live-cell imaging through thick specimens (50...
Imaging volumes as thick as whole cells at three-dimensional (3D) super-resolution is required to re...
Diffraction limits the biological structures that can be imaged by normal light microscopy. However,...
AbstractBiological structures span many orders of magnitude in size, but far-field visible light mic...
Applicability to living specimens and genetically encodable tagging has made fluorescence microscopy...
Fluorescence photoactivation localization microscopy (FPALM) images biological structures with subdi...
ABSTRACT Biological structures span many orders of magnitude in size, but far-field visible light mi...
Three-dimensional (3D) fluorescence microscopy has become one of the major tools for investigating l...
Quantitative three dimensional maps of cellular structure, activity and function provide the key to ...
Abstract Three-dimensional (3D) reconstruction of thick samples using superresolution fluorescence m...
The phenomenon of diffraction limits the resolution in fluorescence imaging. While biological struct...
Due to the diffraction limit of light, the resolution of fluorescence light microscopy is limited to...
We propose clean localization microscopy (a variant of fPALM) using a molecule filtering technique. ...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We demonstrate three-dimensional (3D) super-resolution live-cell imaging through thick specimens (50...
Imaging volumes as thick as whole cells at three-dimensional (3D) super-resolution is required to re...
Diffraction limits the biological structures that can be imaged by normal light microscopy. However,...
AbstractBiological structures span many orders of magnitude in size, but far-field visible light mic...
Applicability to living specimens and genetically encodable tagging has made fluorescence microscopy...
Fluorescence photoactivation localization microscopy (FPALM) images biological structures with subdi...
ABSTRACT Biological structures span many orders of magnitude in size, but far-field visible light mi...
Three-dimensional (3D) fluorescence microscopy has become one of the major tools for investigating l...
Quantitative three dimensional maps of cellular structure, activity and function provide the key to ...
Abstract Three-dimensional (3D) reconstruction of thick samples using superresolution fluorescence m...
The phenomenon of diffraction limits the resolution in fluorescence imaging. While biological struct...
Due to the diffraction limit of light, the resolution of fluorescence light microscopy is limited to...
We propose clean localization microscopy (a variant of fPALM) using a molecule filtering technique. ...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
We demonstrate three-dimensional (3D) super-resolution live-cell imaging through thick specimens (50...