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. Author manuscript; available in PMC: 2018 Dec 28.
Published in final edited form as: Parasitology. 2016 Nov 21;144(4):459–463. doi: 10.1017/S0031182016001918

Fig. 2.

Fig. 2.

Western blot analysis using sera with potential cross-reactivity. (A) The crude A. cantonensis worms antigen extract was loaded at a concentration of: 100 ng per well (lane 1), 75 ng per well (lane 2) and 50 ng per well (lane 3). The blots were incubated with pooled serum samples prepared from cases with Toxocara infection, NHS and A. cantonensis infection. (B) Individual Western blot strips were prepared from the crude antigen extract loaded at a concentration of 35 ng per well. The strips were tested against the following sera: 1-NHS; 2–8 cases of Echinococcus infection; 9–12 Strongyloides infection; 13–16 Toxocara infection; 17–32 Angiostrongylus infection. NHS, normal human sera.