RNA (100 ng) from vehicle or lewisite-exposed skin samples was hybridized overnight at 65°C to the nanoString nCounter mouse Inflammation V2 panel (nanoString Technologies, Seattle, WA, USA) comprising 254 genes. Hybridized samples were then immobilized onto an nCounter cartridge and imaged on an nCounter SPRINT Profiler (nanoString Technologies) as previously described (25 (link)). Data were analyzed with nSolver Analysis Software (nanoString Technologies). The threshold for significant differential expression was |1| for log fold change and p<0.05 for t-test significance.
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