Experiments were conducted using the following primary antibodies: anti-p53 antibody (1:1,000 working dilution), anti-BCL-xL antibody (Cell Signaling Technology, 2764 S, 9, 1:1,000 working dilution) and anti-caspase 3 antibody (Proteintech, 19677-1-AP, 1:1,000 working dilution) as indicated. The secondary antibodies HRP-conjugated Goat Anti-Mouse IgG (Abbkine, A21010, ATSDE1601, 1:2,000 working dilution), HRP Goat Anti-Rabbit IgG (Absin, abs20040, AS004, 1:2,000 working dilution) were used. Bands were visualized by enhanced chemiluminescence detection reagents (Vazyme, E411-04). Bands of western blotting were quantified using ImageJ software.

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