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. 2021 Oct 4;49(19):11224–11240. doi: 10.1093/nar/gkab842

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© The Author(s) 2021. 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 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 1. — USP37 interacts with BLM. (A) 293T cells were transfected with HA-tagged cDNA as indicated and then treated with 10 μM MG132 for 4 h before performing Co-immunoprecipitation (Co-IP) assays. Immunoblotted with the indicated antibodies. (B) Interaction between transfected Myc-tagged-BLM and endogenous USP37. Lysates from HEK293T cells expressing Myc-BLM were subjected to co-IP assays using the USP37 antiboddy and Myc antibody followed by western blot analysis. (C, D) Interaction between endogenous USP37 and BLM. HEK293T cell were collected and subjected to immunoprecipitation using control IgG, (C) USP37 antibody or (D) BLM antibody. Blots were probed with the indicated antibodies.