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Reverse transcription-quantitative PCR was utilized to identify the appearance degrees of miR-429 and DUSP4, and also to confirm the transfection effectiveness of miR-429 mimic and DUSP4 overexpression plasmid. Cell Counting Kit-8 assay had been useful to measure the inhibition rate of cells. Western blotting had been performed to see the phrase levels of DUSP4 protein, apoptosis-related proteins and proteins related to the JNK signaling path. Dual-luciferase reporter assay was pe