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These finding suggest that depressed GSH levels may be associated with enhanced protective mechanism to oxidative stress in AMI
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Three-micron sections were prepared and mounted on slides, followed by deparaffinization and immunofluorescent staining according to a standard protocol as follows: For deparaffinization, the paraffin-embedded sections were placed at 60 C for at least 30 min, incubated twice in xylene (5 minutes each), and then transferred into 100% ethanol (2 minutes), 100% ethanol (2 minutes), 90% ethanol (1 minute), 80% ethanol (1 minute), and 70% ethanol (1 minute) at room temperature
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After staining, the media was removed from cells, cells were washed three times with PBS, and scraped into 300 L of FACS buffer
