EVAg

RNA extracted from infected cell culture supernatant of Zika virus strain MRS_OPY_Martinique_PaRi_2015. Virus Provenance Martinique 2015,

Development and production of Diagnostic systems with positive control for arboviruses (RUO)

genomic RNA from culture supernatant of UVE/SARS-CoV-2/2021/FR/1299-ex SA. 100µL containing E+04 copies/µl provided in AVE buffer + RNA carrier.

genomic RNA from culture supernatant of SARS-CoV-2/2021/FR/7b (lineage B 1. 1 .7, ex UK). 100µL containing 1.25E+04 copies/µl provided in AVE buffer + RNA carrier.

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,

Subgenomic Amplicons for Zika virus strain H/PF/2013. It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after transfection into cells.

Subgenomic Amplicons for Zika virus strain Dak84 (derived from genbank sequence KU955592). It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after transfection into cells

Subgenomic Amplicons for Japanese encephalitis virus strain CNS769_Laos_2009. It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after 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.

RNA extracted from infected cell culture supernatant of Pichinde virus. Virus Provenance Colombia, 1965,

RNA extracted from infected cell culture supernatant. Virus Provenance: St Martin, French Caribbean