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Subsequently, according to the method described in the previous study ( 2.7 Immunofluorescence (IF) After transcardial perfusion in mice, brain tissues were harvested and pretreated with gradient dehydration in 20% and 30% sucrose solutions at 4C (to reduce ice crystal damage), then embedded in optimal cutting temperature compound and sectioned for 20 m thickness using cryostat

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BACH1 directly modulates numerous critical inflammatory and repairrelated genes in musclederived macrophages following cardiotoxin injury, including IGF1, SLC40A1, IL6, IL10, GDF3, PPARG, DUSP1, and CEBPB, potentially elucidating the delayed muscle regeneration phenotype observed in BACH1 KO mice