Las4000epuvmini

After iPS-MLs or SH-SY5Y cells were cultured with the appropriate TTRs for 3 days, culture supernatants were mixed with sample buffer (Bio-Rad Laboratories, Hercules, CA, USA) containing 2-mercoptoetanol, and boiled at 95°C for 5 min. Resultant samples were separated by SDS-PAGE and transferred to PVDF membranes (Bio-Rad). Polyclonal rabbit anti-human TTR antibody (Dako; diluted 1:1000) was used as the primary antibody, and polyclonal goat anti-rabbit antibody conjugated with HRP (Dako; diluted 1:5000) as the secondary antibody. The reaction was visualized using ECL prime reagents (GE Healthcare, WI, USA), and detected using a LAS-4000EPUVmini (GE Healthcare).

U251MG cells (10⁵ cells/1000 µL/well) were cultured in DMEM/F12 culturing condition (serum-free medium as recently described [14 (link)]) using a 24-well plate (Corning) for 72 h. U251MG Cells were lysed in ice-cold lysis buffer containing phosphatase inhibitor (CST). Whole proteins from cultured cells were extracted using cell lysis buffer following the manufacturer’s instructions (CST). Proteins were separated by SDS-PAGE in a 10% resolving gel and electro-transferred onto polyvinylidene difluoride membranes (Merck). Membranes were blocked in 3% skim milk (GE Healthcare, Minato-ku, Tokyo, Japan) in TBS-T at ambient temperature for 1 h with agitation, and incubated with the following primary antibodies overnight at 4 °C: rabbit polyclonal anti-RPS6 antibody (1:1000), mouse polyclonal anti-β-actin antibody (1:1000), rabbit polyclonal anti-STAT3 (1:1000), rabbit polyclonal anti-p-STAT3 (Tyr705) (1:1000), rabbit polyclonal anti-SOX2 (1:1000), and mouse monoclonal anti-Nestin (1:1000) antibodies. After three washes, the membranes were incubated with horseradish peroxidase-conjugated secondary antibody (rabbit: GE Healthcare, mouse: GE Healthcare) with 3% skim milk for 1 h. Finally, immunoreactive protein bands were visualized by using ECL select detection reagents (GE Healthcare) and captured using the LAS4000EPUVmini (GE Healthcare).