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. 2024 Jul 17;15(7):508. doi: 10.1038/s41419-024-06905-1

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© The Author(s) 2024

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 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/.

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Fig. 4 — a Percentage of holoclones found in untransduced (JEB-NT), FOXM1- (JEB-FOXM1) or LAMB3-transduced (JEB-LAMB3) JEB-derived primary keratinocyte cultures (see ‘Methods’). b qRT-PCR quantification of the mRNA levels of H1B, H1D, H1E on cells derived from untransduced (JEB-NT), FOXM1- (JEB-FOXM1) or LAMB3-transduced (JEB-LAMB3) JEB-derived primary keratinocyte culture. Expression levels are normalized per GAPDH. c Western analysis on total cell extract derived from NHK, untransduced (JEB-NT) and LAMB3-transduced (JEB-LAMB3) JEB-derived primary keratinocyte cultures. Molecular weight indicators are shown. d Western analysis on total cell extract derived from untransduced (JEB-NT), FOXM1- (JEB-FOXM1) JEB-derived primary keratinocyte cultures. Molecular weight indicators are shown.