Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA
Fig 1
Reactivity of the iELISA using recombinant proteins with horse sera.
Lanes: 1, uninfected horse sera (black circle); 2, sera experimentally infected with B. caballi (red square); 3, sera experimentally infected with T. equi (Grey tri-angle). The cutoff of each recombinant protein is indicated by a bar. The serum samples were collected at day 18 post infection.