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lated group were significantly higher than those in the phosphate-buffered saline-stimulated group (normal control group). The high conservation at specific amino acid sites and the high immunogenicity of the C-terminal of PvRAMA indicate the presence of conserved epitopes able to generate broadly reactive humoral and cellular immune responses. These findings support the potential of PvRAMA to serve as a vaccine candidate against P. vivax infection. The high conservation at specific amino acid sites and the high immunogenicity of the C-te

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