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.
Freeze-dried Tick Borne Encephalitis Virus, strain UVE/TBEV/2013/FR/32.11 WT-PCR, complete ORF sequence. It was produced by ISA method from infectious clone derived from Oshima 5.10 strain (genbank sequence KF623542)
Lyophilized encapsidated RNA for SARS-CoV-2 (2019-nCoV) real time RT-PCR targeting region of the N (CUB) gene, for 100 Rxns (Target designed by Charité Universitätsmedizin Berlin).
The encapsidated RNA has been stabilized to serve as positive control for extraction and real time RT-PCR. Extraction is mandatory before use in real time RT-PCR. SOPs in the attached pdf.
For RUO (Research Use Only)