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Remaining N1ICD at indicated time detected by western blotting assay in Capan1 with overexpressed USP10 followed by N1DARP introduction after treatment with CHX. i Co-IP followed by western blotting assay using Capan1 with USP10 knockout to detect the effect of USP10 on the interaction between N1DARP and N1ICD. The data represent three independent experiments. * P < 0.05 by one-way ANOVA ( h ).

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