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To improve the weak immunogenicity of peptide P277, the recombinant expression plasmid pET28-Hsp65-6×P277 was constructed by inserting 5×P277 which was amplified by PCR into the vector pET28-Hsp65-P277. It was transformed into Escherichia coli BL21 (DE3) and the fusion protein (Hsp65-6×P277) was expressed effectively as soluble protein after inducing by lactose. The fusion protein was purified by...
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