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

Published: 5 September 2017| Version 1 | DOI: 10.17632/4nh2ts7rdc.1
Contributor:
Emi Tucker

Description

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.

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Contact etucker3@illinois.edu for protocols.

Categories

In Vitro Toxicology

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