“…Then 1 mL of blocking buffer (0.5% casein, w/v) was added, and the solution was stirred for 2 h. Next, the mixture was centrifuged at 8,000 × g for 25 min to remove the blocking agent and excess antibody. The precipitate was collected and washed with gold-labeled resuspension buffer three times (20 mM Tris [pH 8.2], 0.1% PEG, 0.1% Tween, 5% sucrose, 5% trehalose, 0.2% BSA, and 5% Brij) (Jiang, Zeng, et al, 2018). Finally, the mAb was reconstituted to a volume of 1 mL with gold-labeled resuspension buffer including 0.02% NaN 3 and stored at 4°C until use (Kong, Xie et al 2017;Xie et al, 2018).…”