Discover the SciOpen Platform and Achieve Your Research Goals with Ease.
Search articles, authors, keywords, DOl and etc.
Cryo-electron tomography (cryo-ET) can provide invaluable insights into subcellular structures in their native environment at molecular resolution. Cryo-focused ion beam (cryo-FIB) has been widely adopted to obtain thin lamellae of cells suitable for tomographic data acquisition. However, its application to tissue samples faces significant limitations. The larger sample size extends milling time, reducing sample preparation throughput. Furthermore, the need for repeated, intricate lift-out procedures adds considerable time and complexity to the workflow. The serial lift-out technique, which can prepare multiple lamellae, increases throughput and better preserves the structural integrity of the tissue sample. Here we outline the workflow of the optimized serial lift-out method and provide a detailed protocol for its implementation, exemplified by a vitrified mouse liver tissue sample.
This article is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Comments on this article