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. 2021 May 22;18:19. doi: 10.1186/s12950-021-00286-4

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© The Author(s) 2021

Open AccessThis 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. 8 — Nuclear-to-cytoplasmic redistribution of AIM2 in cigarette smoke extract- (CSE-) stimulated HBEC30KT cells. a: Representative Western blots analysis of AIM2 in whole cell lysate(W), cytoplasmic (c) and nuclear fractions (N) (n = 2). b Comparison of band abundance between CSE-stimulated and control. Band abundance was normalized to the corresponding band in the whole cell lysate and adjusted to GAPDH (cytoplasmic) or Lamin B1 (nuclear) expression. c Representative confocal images of HBEC30KT, control vs. CSE-stimulated (n = 2). Green: mouse mAb (Ab5); Red: rabbit pAb (Ab1). Blue: DAPI. Scale bars are in micrometers