Fig. 1.

Viral vector construct displaying the key features of TuMv-GFP used in this research to clone and express camelied anti-VEGFR2 nanobody. 35S promoter Cauliflower mosaic virus (CaMV) 35S promoter, 5′ and 3′ UTR 5′ and 3′ untranslational region, P1 RNA-silencing suppressor, Hc-Pro helper component proteinase protein, P3 protein 3, 6K1 6 kDa 1 protein, CIP cylindrical inclusion protein, 6K2 6 kDa 2 protein, NIa-VPg viral genome-linked protein of nuclear inclusion protein a, NIa-Pro proteinase domain of Nia, NIb nuclear inclusion protein b, CP the virus coat protein gene. This vector double digested with NcoI and NheI restriction enzymes to remove the GFP gene from it