Methylmercury reduces migratory capability, inhibits proliferation, and induces oxidative stress in an immortalized human trophoblast cell line

Raw data from a migration scratch assay, a proliferation assay, a viability assay, and RT-PCR using first trimester immortalized human trophoblast cells (HTR8/SV-neo) that were treated with methylmercury at 0, 0.01, 0.1 and 1 ug/mL.本数据集包含的原始数据，来自经浓度分别为0、0.01、0.1及1 μg/mL的甲基汞处理的妊娠早期永生化人滋养层细胞（HTR8/SV-neo）的四类实验，分别为细胞划痕迁移实验（migration scratch assay）、细胞增殖实验、细胞活力实验与逆转录聚合酶链式反应（RT-PCR）。