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Near-isotropic, aligned volume electron microscopy (eFIB-SEM) of Mouse hippocampus (jrc_mus-hippocampus-2)

dataset
posted on 2025-05-22, 18:10 authored by CellMap Project TeamCellMap Project Team, Sambashiva Banala, Sebastian E. Brauchi, Severine Chaumont-Dubel, David E. Clapham, Fei Deng, Vincent Dupuy, Melanie Freeman, Harald HessHarald Hess, Justin Houser, Tom Kirchhausen, Luke LavisLuke Lavis, Yulong Li, Song Pang, H. Amalia Pasolli, Silvia Sanchez-Martinez, Shu-Hsien SheuShu-Hsien Sheu, Srigokul Upadhyayula, Deepika Walpita, Jinxia Wan, C. Shan XuC. Shan Xu
<p dir="ltr"><b>Sample</b>: 2–3 month old male mouse, strain: C57BL/6J from Jackson Lab.</p><p dir="ltr"><b>Sample Description</b>: This dataset was acquired from the CA1 region of the mouse hippocampus using a hybrid fixation and staining protocol optimized for primary cilia visualization. Tissue from a 2–3-month-old male C57BL/6J mouse was perfused with 3% paraformaldehyde, sectioned, and processed through high-pressure freezing in 1-hexadecene. The sample was freeze-substituted in osmium tetroxide, uranyl acetate, and either 3-amino-1,2,4-triazole or imidazole, and embedded in Durcupan resin. Sample preparation was performed by Shu-Hsien Sheu. Imaging and post-processing were completed by C. Shan Xu (Yale), Gleb Shtengel, and Harald Hess (HHMI/Janelia).</p><p dir="ltr"><b>Protocol</b>: Two datasets were acquired from the CA1 region of the mouse hippocampus using a hybrid fixation and staining protocol optimized for primary cilia visualization. 2–3-month-old male C57BL/6 mice were perfused with 3% paraformaldehyde and post-fixed in modified PFA buffer for 2 hours. Tissue was rinsed in 400 mOsM buffer and sectioned (100 µm) on a vibratome. Sections were fixed overnight in 1% PFA and 2% glutaraldehyde. 2 mm punches were high-pressure frozen in 1-hexadecene, freeze-substituted in osmium tetroxide, uranyl acetate, and either 3-amino-1,2,4-triazole or imidazole. Samples were embedded in Durcupan resin.</p><p dir="ltr"><b>Contributions</b>: Sample prepared by Shu-Hsien Sheu. Imaging and post-processing by C. Shan Xu (Yale), Gleb Shtengel, and Harald Hess(HHMI/Janelia).</p><p dir="ltr"><b>Acquisition ID</b>: jrc_mus-hippocampus-2</p><p dir="ltr"><b>Voxel size (nm)</b>: 8 x 8 x 8 (x, y, z)</p><p dir="ltr"><b>Data dimensions (µm)</b>:<b> </b>44.98 x 44.9 x 55.06 (x, y, z)</p><p dir="ltr"><b>Imaging start date</b>: 2017-10-04</p><p dir="ltr"><b>Imaging duration (days)</b>: 8</p><p dir="ltr"><b>Landing energy (eV)</b>: 1100</p><p dir="ltr"><b>Imaging current (nA)</b>: 1</p><p dir="ltr"><b>Scanning speed (MHz)</b>: 1.250</p><p dir="ltr"><b>Dataset URL</b>: <a href="https://data.janelia.org/9YeduS" rel="noreferrer" target="_blank">s3://janelia-cosem-datasets/jrc_mus-hippocampus-2/jrc_mus-hippocampus-2.zarr/recon-1/em/</a></p><p dir="ltr"><b>Visualization Website</b>: <a href=" https://openorganelle.janelia.org/datasets/jrc_mus-hippocampus-2" rel="noreferrer" target="_blank">https://openorganelle.janelia.org/datasets/jrc_mus-hippocampus-2</a></p><p dir="ltr"><b>Publication</b>:<b> </b>Sheu, et al., 2022<b>; </b>Xu et al., 2017</p><p><br></p>

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