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For immunofluorescence, sections were washed with PBS at room temperature twice for 10 min, followed by incubation in blocking buffer (5% fish gelatine, 0.5% Triton in PBS) at room temperature for 1 h before incubation with the primary antibodies (see Supplementary Table 4 for primary antibodies used in this study) diluted in the blocking buffer at 4 C overnight

Toxicological sciences : an official journal of the Society of Toxicology , 147 (2), 466-474

Reconstitution Quick Reference Math: 50,000 mcg / 3 mL = 16,667 mcg/mL (16.67 mg/mL)

Hiroyuki Ueki (KEYENCE, Osaka, Japan) for the technical guidance and assistance on immunofluorescence microscopy

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