Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy
Summary: This protocol describes how to prepare intact mouse cochleae for serial block-face scanning electron microscopy (SBEM). The detailed workflow includes cochlea fixation, en bloc staining, resin embedding, X-ray microscopy-guided trimming and SBEM data acquisition. This protocol allows large-...
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2021-06-01
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doaj-ed285b137979403285dbc87a080d36ac2021-06-21T04:25:30ZengElsevierSTAR Protocols2666-16672021-06-0122100515Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopyYan Lu0Fangfang Wang1Haoyu Wang2Philipp Bastians3Yunfeng Hua4Shanghai Institute of Precision Medicine, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaShanghai Institute of Precision Medicine, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Corresponding authorShanghai Institute of Precision Medicine, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaZEISS Research Microscopy Solutions, Shanghai, ChinaShanghai Institute of Precision Medicine, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Corresponding authorSummary: This protocol describes how to prepare intact mouse cochleae for serial block-face scanning electron microscopy (SBEM). The detailed workflow includes cochlea fixation, en bloc staining, resin embedding, X-ray microscopy-guided trimming and SBEM data acquisition. This protocol allows large-scale, nanometer-resolution three-dimensional imaging of subcellular structures in a targeted tonotopic range of the cochlea and enables fast volumetric scan at submicron resolution using a compact X-ray microscope.For complete details on the use and execution of this protocol, please refer to Hua et al. (2021).http://www.sciencedirect.com/science/article/pii/S2666166721002227Cell BiologyMicroscopyNeuroscience |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yan Lu Fangfang Wang Haoyu Wang Philipp Bastians Yunfeng Hua |
spellingShingle |
Yan Lu Fangfang Wang Haoyu Wang Philipp Bastians Yunfeng Hua Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy STAR Protocols Cell Biology Microscopy Neuroscience |
author_facet |
Yan Lu Fangfang Wang Haoyu Wang Philipp Bastians Yunfeng Hua |
author_sort |
Yan Lu |
title |
Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy |
title_short |
Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy |
title_full |
Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy |
title_fullStr |
Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy |
title_full_unstemmed |
Large-scale 3D imaging of mouse cochlea using serial block-face scanning electron microscopy |
title_sort |
large-scale 3d imaging of mouse cochlea using serial block-face scanning electron microscopy |
publisher |
Elsevier |
series |
STAR Protocols |
issn |
2666-1667 |
publishDate |
2021-06-01 |
description |
Summary: This protocol describes how to prepare intact mouse cochleae for serial block-face scanning electron microscopy (SBEM). The detailed workflow includes cochlea fixation, en bloc staining, resin embedding, X-ray microscopy-guided trimming and SBEM data acquisition. This protocol allows large-scale, nanometer-resolution three-dimensional imaging of subcellular structures in a targeted tonotopic range of the cochlea and enables fast volumetric scan at submicron resolution using a compact X-ray microscope.For complete details on the use and execution of this protocol, please refer to Hua et al. (2021). |
topic |
Cell Biology Microscopy Neuroscience |
url |
http://www.sciencedirect.com/science/article/pii/S2666166721002227 |
work_keys_str_mv |
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_version_ |
1721369053859151872 |