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. 2023 Jul 8;14(7):408. doi: 10.1038/s41419-023-05938-2

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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. 3 — A The endogenous interaction among UBE2S, TRIM21 and LPP in BCa cells was determined by performing co-IP and western blot assays. Anti-UBE2S (14115-1-AP, Proteintech), anti-TRIM21 (12108-1-AP, Proteintech) and anti-LPP (25045-1-AP, Proteintech) were used for Co-IP (each 2 μg). B Representative immunofluorescence images of UBE2S, TRIM21 and LPP colocalization in the nucleus and cytoplasm of BCa cells. Scale bars: white, 25 μm. DAPI was used to label the cell nucleus. C UBE2S, TRIM21 and LPP protein levels in UBE2S-silenced or UBE2S-overexpressing BCa cells. D TRIM21 and LPP protein levels in TRIM21-silenced BCa cells.