Ultrasensitive chemiluminescence kit

The HDPCs (2 × 10⁵) were treated under different conditions for different time points. The EMPs (1 µM) were also added to the HDPCs as an extra control group. Then the cells were harvested and lysed in 200 µL lysis buffer (Beyotime, Shanghai, China) and centrifuged (12 000 rpm for 10 min, at 4°C). The protein concentration was evaluated with a BCA kit (Solarbio, Beijing, China). The protein was mixed with 5× loading buffer and heated at 95°C for 5 min, separated by precast PAGE gel (Beyotime, Shanghai, China) and transferred to polyvinylidene fluoride membranes. After blocked at room temperature for 15 min, then incubated with the primary antibody (DSPP, DMP-1, Smad2/3, c jun, p-c jun, c fos, p-c fos, c jun B) (Santa Cruz, California, USA), [p-ERK1/2, ERK1/2, alkaline phosphatase (ALP), p-Smad2/3, GAPDH] (Beyotime, Shanghai, China). Then, the membranes were incubated with the goat anti-rabbit IgG-HRP secondary antibody or goat anti-mouse IgG-HRP secondary antibody for 1 h, respectively. Then, an ultrasensitive chemiluminescence kit (Beyotime, Shanghai, China) was used to detect the protein bands. A chemiluminescence imager (Bio-Rad, California, USA) was used to scan the protein bands. The Image Lab software was used to analyze the relative protein expression levels.