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. 2019 Apr 30;47(12):6130–6144. doi: 10.1093/nar/gkz312

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© The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 6. — Zfp217 interacts with YTHDF2. (A) CoIP and reverse CoIP analysis of interaction between Zfp217 and YTHDF2 in 3T3L1 cells with or without MDI treatment for 2 days using antibodies against the endogenous proteins (n = 3). IgG was used as a negative control. (B) Protein expression level of Zfp217 and YTHDF2 in cytoplasmic and nuclear fractions was analyzed by western blot (n = 3). (C and D) Subcellular localization of Zfp217 and YTHDF2 in 3T3L1 cells with or without MDI treatment for 2 days. 3T3L1 cells were immunostained with antibodies against Zfp217 and YTHDF2. DAPI was used for nuclear staining. Cells analyzed with a confocal laser scanning microscope (63× magnification) with Z-scan analysis.