TTX was diluted in culture medium to 30 μM. Staurosporine was prepared as stock in DMSO and then diluted in culture medium. In assays that exceeded 24 h, treatments were replaced daily. In vitro migration and invasion were determined using wound healing and Matrigel assays [16 (link)]. Apoptosis was determined using DeadEnd fluorometric TUNEL assay (Promega). Cell viability and proliferation were determined using trypan blue and MTT assays [16 (link)].
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