EVAg

Purified Recombinant Envelope Domain III Protein (N-terminal SNAP-Tagged, C-terminal His-Tagged) expressed in Drosophila S2 Cells

In vitro transcribed RNA for a specific yellow fever real time RT-PCR (Domingo C. et al, JCM, 2012). Product only available via TNA.

Recombinant protein produced in E. coli and purified to homogeneity. Fused with a Hexa-Hisitidine tag.

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.

Quantified freeze-dried genomic standard for molecular detection of Yellow fever virus, made of an inactivated culture supernatant of Vaccinal strain 17D with quantified genomic titre.

Set of primers and probes to detect viral RNA of Yellow fever virus on diagnostic level. Suitable with the EVD-labnet / EVAg EQA of molecular diagnostics on Chikungunya, Dengue, West Nile, Yellow fever and Zika virus 2019.