EVAg

Entry Plasmid of FIPV Nsp5 (protease), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of FIPV Nsp14, Full gene (exonuclease), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of FIPV Nsp14, Full gene (exonuclease), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp7, Full gene (UNK), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp9, Full gene (UNK), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp10, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp2, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp14, Full gene (exonuclease), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp16, Full gene (2'O MTase), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of AIBV Nsp16, Full gene (2'O MTase), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of EqTV Nsp15+16, Full genes (Endonuclease+Methyltransferase), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of EqTV Nsp15+16, Full genes (Endonuclease+Methyltransferase), in fusion with a C-Terminal His tag coding sequence

Expression Plasmid of EqTV Macro Domain, in fusion with a N-Terminal His tag coding sequence for expression in E. coli

Expression Plasmid of EqTV Nsp8, Full gene (RNAbinding), in fusion with a N-Terminal His tag coding sequence for expression in E. coli

Expression clone of MHV nsp3 Domain, in fusion with a Nterminal His Tag coding sequence

Expression clone of MHV nsp3 Domain (UNK+UNK+Protease), in fusion with a N terminus coding sequence

Infectious Subgenomic Amplicons Reverse Genetic system for Zika virus strain Dak84 (derived from genbank sequence KU955592). 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 cells,

Infectious Subgenomic Amplicons Reverse genetic system for Zika virus strain H/PF/2013. 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 cells,

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.

Entry Plasmid of TGEV Nsp4, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp9, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp9, Full gene (UNK), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp8, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp8, Full gene (UNK), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp7, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence