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. 2023 Sep 12;24:540. doi: 10.1186/s12864-023-09649-y

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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 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — miR-128-3p inhibited the differentiation of chicken intramuscular adipocytes. A, B Relative mRNA levels of cell proliferation-related genes (FABP4, FASN and CEBPA) after miR-128-3p overexpression or interference. C Representative images of Oil Red O staining in intramuscular adipocytes transfected with the miR-128-3p mimic, miR-128-3p inhibitor or corresponding NC (this image was acquired with a 20 × objective, and an enlarged image is shown in the bottom left corner of the image). D, E Semiquantitative assessment of Oil Red O absorbance at 450 nm. F, G The triglyceride content was determined by measurement of the absorbance at 500 nm after miR-128-3p overexpression or interference