Fig. 2From: Mapping of the complement C1q binding site on Trichinella spiralis paramyosinDetermination of the TsPmy fragment that binds to C1q by ELISA. ELISA plate was coated with C1q (b) or BSA (c) (5 μg/ml), then incubated with different concentrations (0, 2.5, 5, 10 and 20 μg/ml) of each recombinant fragment of TsPmy (1-315aa, 286-600aa and 571-885aa) (a), then detected with anti-His mAb (1:1,000) (b, c). Results were repeated three times. Data are shown as mean ± SEMBack to article page