EVAg

Infectious Subgenomic Amplicons Reverse genetic system for chimeric virus CH-17D / ZIKV. It consists of three non infectious overlapping DNA fragments (cloned into pUC57 vector) . These products enable to obtain infectious RNA virus after amplification by PCR, and transfection into susceptible cells. The chimeric virus systems were constructed using the yellow fever 17-D vaccine strain as a genetic backbone and by replacing prM/E from this vaccine strain with those of the Asian ZIKV PF epidemic strain.

Expression plasmid for the production of the Nterminal - Domain of ZIKV NS5 (methyltransferase domain). Synthetic gene optimized for E. coli. Coding sequence fused at its 5' with a 6His tag coding sequence

Expression plasmid for the production of the Nterminal - Domain of ZIKV NS5 (methyltransferase domain, amino acids 4-278). Synthetic gene optimized for E. coli. Coding sequence fused at its 5' with a 6His tag coding sequence

complete gp without transmembrane domain, linked to double Strep-Tag; WE isolate

Plasmid for the expression of the LCMV strain clone 13 L-protein in eukaryotic cells. [also termed pDP061 pC-L_Cl.13(ZH)_Bsm]