After three washes with the wash buffer, 50 μL/well of substrate buffer was added, and the plates were incubated at room temperature for 15 min. The reaction was terminated with 50 μL/well of 4 N sulfuric acid. Absorbance was recorded at 492 nm using an ELISA plate reader (Labsystems Multiskan Ex, Thermo Fisher Scientific Inc., Walthan, MA). The results are expressed as follows: affinity index (AI) = M KSCN needed to displace 50% of the bound antibodies. A fixed amount of 5 LD50 of selleck C. d. terrificus venom and various dilutions of antivenoms were incubated for 30 min at 37 °C. Venom samples incubated only with PBS buffer were used as controls. After incubation, 500 μL aliquots of the mixtures were intraperitoneally

injected in the mice. Five mice were used per mixture. The death/survival ratio was recorded 48 h after the injection. ED50 was estimated by probit analysis ( Finney, 1992). The obtained data were subject http://www.selleckchem.com/erk.html to a one-way ANOVA, followed by the Dunn’s multiple comparison

test. Differences were considered to be significant for P < 0.05. The protein concentrations (μg/mL) and lethality (LD50) of the C. d. terrificus, C. d. collilineatus, C. d. cascavella and C. d. marajoensis venoms used in this work were determined by using the bicinchoninic acid method and the LD50 in mice ( Table 1). The electrophoretic profiles of the venoms were determined by the polyacrylamide electrophoresis ( Fig. 3a). Anacetrapib Previous studies have shown that the major venom in the Crotalus species is crotoxin ( Santoro et al., 1999). Although some differences were noted, mainly in terms of the electrophoretic mobility of the protein bands and their intensity, the venoms were similar overall in the four Crotalus subspecies. The differences noted, usually in the concentrations of particular components, correlated with the ages of the

snake donors at the time of venom collection as well to the particular ecological regions from which the specimens were collected. C. d. terrificus crude venom (20.0 mg) was applied to a Mono Q HR 5\5 column (Amershan Pharmacia Biotech AB, Uppsala, Sweden), which had been previously equilibrated with pH 7.4 Tris buffer and eluted with a linear gradient of NaCl (0.0–1.0 M) in pH 7.4 Tris buffer. The chromatography resulted in 11 peaks ( Fig. 2a). Peak 2 was represented by only one 15 kDa protein band, whereas peaks 5 contained a majority band of 15 kDa and the other of 30 kDa ( Fig. 2b). The activity of PLA2, as assayed on synthetic substrate l-α-phosphatidylcholine, was detected only in peak 2 (data not shown). Upon “dot blotting” using specific mouse anti-crotoxin as the primary antibody, peak 5 reacted positively, indicating the presence of crotoxin (data not shown). Equal samples of the C. d. terrificus, C. d. collineatus, C. d. cascavella and C. d. marajoensis venoms were treated with SDS under reducing conditions and separated by polyacrylamide gel electrophoresis (upper gel, 5%; lower gel, 12.5%).