“…In order to detect TSWV particles in infected tomato plants and individual viruliferous thrips, TAS-ELISA was carried out as previously described (Sakurai et al, 1998) using commercially available polyclonal antibody (PAb, American Type Culture Collection, Manassas, VA, USA) for coating the wells, and monoclonal antibody (MAb, Agdia Inc., Elkhart, IN, USA) for detecting TSWV-N protein. The concentration of PAb was 1 mg/ml in a carbonate buffer (0.05 M sodium carbonate, pH 9.6), and that of MAb was 0.25 mg/ml in a phosphate-buffered saline (PBS, 0.14 M NaCl, 1 mM KH 2 PO 4 , 8 mM Na 2 HPO 4 , 2.5 mM KCl, pH 7.4), including 0.05% Tween 20, 2% polyvinylpyrrolidone (PVP-40) and 0.2% bovine serum albumin.…”