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. 2024 Jul 23;14:16895. doi: 10.1038/s41598-024-66473-4

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© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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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ACE2 and CFTR co-immunoprecipitate in both basal cells and differentiated BCi.NS1.1 (d-BCi) epithelia. (a) A representative western blot image shows both untreated basal (b-BCi) cells and differentiated (d-BCi) cells expressing CFTR and ACE2. β-actin was used for equal loading of protein. (b) A representative western blot image showing CFTR co-immunoprecipitating with ACE2 from both basal (b-BCi) and differentiated (d-BCi) epithelia lysates. Normal rabbit serum (NRS) was used as the control. Western blot data represent the results of three independent experiments.