In experiments involving EAs, the coverslips were moved to 4 C to avoid phagocytosis, and exterior EAs were recognized from inner EAs by labeling with a second fluorescent anti-IgG (internalized EAs aren’t labeled)
In experiments involving EAs, the coverslips were moved to 4 C to avoid phagocytosis, and exterior EAs were recognized from inner EAs by labeling with a second fluorescent anti-IgG (internalized EAs aren’t labeled). 2.6. at a focus of 900 M, and kept at ?20 C. Ahead of use peptides had been diluted 4-Aminohippuric Acid to…