Abstract
Eimeria acervulina was isolated from chicken at Hebei province, China. The gene of merozoite surface antigen 3-1E was amplified and cloned into pET28a(+) vector and then transformed into Escherichia coli BL21 strain. Results showed that 3-1E fusion protein band of about 22 kDa was identified by SDS-PAGE. Western blot analysis indicated that the recombinant protein specifically reacted with E. acervulina polyclonal antibody.
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This research was supported by grants from the National Natural Science Foundation of China (grant number: 30571394) and the National Natural Science Foundation of Hebei province (grant number: C2007000523).
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Yuelan Zhao, Chengmin Wang, and Yanmin Lu contributed equally to this work.
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Zhao, Y., Wang, C., Lu, Y. et al. Prokaryotic expression and identification of 3-1E gene of merozoite surface antigen of Eimeria acervulina . Parasitol Res 109, 1361–1365 (2011). https://doi.org/10.1007/s00436-011-2381-9
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DOI: https://doi.org/10.1007/s00436-011-2381-9