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. 2023 Mar 30;13(4):623. doi: 10.3390/biom13040623

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© 2023 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Localization of SPE-38::wrmScarlet-I visualized by red fluorescent signal to membranous organelles (MOs) in spermatids. (A–C) Imaging of the same control spermatids dissected from him-5(e1490) males. (A) Single confocal section of control spermatids. (B) Bright field image of control spermatids. (C) Merge of (A,B). (D–F) Imaging of spe-38::wrmScarlet-I; him-5(e1490) spermatids dissected from males. (D) Single confocal section of spe-38::wrmScarlet-I; him-5(e1490) spermatids. (E) Bright field image of spe-38::wrmScarlet-I; him-5(e1490) spermatids. (F) Merge of (D,E). Yellow scale bars, 5 µm.