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. 2023 Nov 13;12:269. doi: 10.1038/s41377-023-01300-5

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a Whole slide image of the mouse kidney tissue section captured with the E2E-BPF microscope. Magnified images from the standard (b, d) and E2E-BPF (c, e) microscopes of the regions are marked with yellow dashed lines in (a). The E2E-BPF microscope could clearly visualize the structures across various depths, without serial refocusing