research-paper | 12-August-2019
were randomly selected from each group, and the percentage of positive cells was calculated for statistical analysis.
To further clarify the location and intensity of caspase 3, 8 and 9 expression, immunohistochemical staining was performed in the exposure groups and the sham group. Anti- caspase 3, 8 and 9 antibodies (1:100; Bioworld Technology, USA), which were produced in rabbits, were the primary antibodies, and a polink-2 plus polymer horseradish peroxidase (HRP) detection system was used in
Acta Neurobiologiae Experimentalis, Volume 79 , ISSUE 2, 155–168