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. 2018 Apr 19;1:34. doi: 10.1038/s42003-018-0039-1

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — The neutralisation of venom-induced prothrombin activation by homologous and heterologous antivenoms and EDTA. The effect of antibodies (150 μg) and EDTA (various molarities from 1 μM to 10 mM) on venom-induced prothrombin activation measured by chromogenic assay. Bars represent end-point absorbances (405 nm). Error bars represent SEM of triplicate measurements. Circles represent individual data points. Asterisks indicate significant reductions in activity compared to venom-only measurements: ***P < 0.001, **P < 0.01, *P < 0.05; one-way ANOVA with Tukey’s HSD post hoc test