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. 2022 Mar 26;37:15333175221085066. doi: 10.1177/15333175221085066

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© The Author(s) 2022

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 4. — Western blots (Upper panel) and qPCR (Lower panel) showing the altered expression of HLA-DQA1 and HLA-DRB1 in the GATA2 and GATA3 (A); ELAVL1 and HNRNPA0 (B); ILF2 and ILF3 (C); NFIB and NFIC (D); and CUX1 (E) shRNA knockdown HMC3 cells. Data for Western blots represents three biologically independent experiments (n = 3). Data for qPCR represents the combination of three biologically independent experiments (n = 3), each in duplicate. α-Tubulin: loading control for Western blot and GAPDH was used as control for qPCR. * P < .05; ** P < .001; and *** P, .0001.