Objective To clone the part gene coding for schistosoma japonicum mucin-like protein into the eukaryotic expression vector pcDNA3.1(+)and to construct a DNA vaccine.Methods TThe fragment of the SjMLP was amplified by PCR and cloned into cloning vector pUCm-T,then it was subcloned into eukaryotic expression vector pcDNA3.1(+).Results The coding region of SjMLP gene was verified after tested by PCR and by sequencing.Conclusion The eukaryotic expression plasmid was successfully constructed,which...