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Therefore, volume EM (vEM) is often crucial for correct interpretation of ultrastructural data. Today, scanning EM (SEM) methods such as focused ion beam (FIB)\u2013SEM are frequently used for vEM analyses. While they allow automated data acquisition, precise targeting of volumes of interest within a large sample remains challenging. Here, we provide a workflow to target FIB-SEM acquisition of fluorescently labeled cells or subcellular structures with micrometer precision. The strategy relies on fluorescence preservation during sample preparation and targeted trimming guided by confocal maps of the fluorescence signal in the resin block. Laser branding is used to create landmarks on the block surface to position the FIB-SEM acquisition. Using this method, we acquired volumes of specific single cells within large tissues such as 3D cultures of mouse mammary gland organoids, tracheal terminal cells in Drosophila melanogaster larvae, and ovarian follicular cells in adult Drosophila, discovering ultrastructural details that could not be appreciated before.<\/jats:p>","DOI":"10.1083\/jcb.202104069","type":"journal-article","created":{"date-parts":[[2021,6,7]],"date-time":"2021-06-07T02:22:07Z","timestamp":1623032527000},"update-policy":"https:\/\/doi.org\/10.1083\/jcb.crossmarkpolicy","source":"Crossref","is-referenced-by-count":58,"title":["High-precision targeting workflow for volume electron microscopy"],"prefix":"10.1083","volume":"220","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9010-533X","authenticated-orcid":true,"given":"Paolo","family":"Ronchi","sequence":"first","affiliation":[{"name":"Electron Microscopy Core Facility, European Molecular Biology Laboratory, Heidelberg, Germany 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