EVAg

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the NTD & RBD of the SARS-CoV-2 gamma variant (P.1) and can be used as positive control for extraction and real time RT-PCR. Extraction is mandatory before use in real time RT-PCR. Packaged for 100 Rxns, for RUO (Research Use Only). SOPs in the attached pdf.

Panel of Freeze-dried SARS-CoV-2 variants (Europe, UK, South Africa, Brazil, Delta). Please note Brazilian variant can not be supplied to private entities

Lyophilized encapsidated RNA (ArRNA) contains a region of the MS2 phage and is used as positive control for extraction and real time RT-PCR. The ArRNA is especially developed to be spiked in whole blood and serum samples. Extraction is mandatory before use in real time RT-PCR. Packaged for 100 Rxns, for RUO (Research Use Only). SOPs in the attached pdf.

Lyophilized encapsidated RNA (ArRNA) contains a region of the MS2 phage and is used as positive control for extraction and real time RT-PCR. The ArRNA is especially developed to be spiked in nasopharyngeal, salivary, urine and stool samples. Extraction is mandatory before use in real time RT-PCR. Packaged for 100 Rxns, for RUO (Research Use Only). SOPs in the attached pdf.

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.

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)

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