EVAg

Freeze-dried human plasma spiked with heat inactivated alphaviruses culture supernatants, (non infectious). The panel contains 15 vials to be tested.

genomic RNA from culture supernatant of Mayaro virus strain UVE/MAYV/1954/TT/TC625. 50µL provided in AVE buffer (without RNA carrier).

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

The service aims at offering the possibility to evaluate the outcome of an infection by a SARS-CoV-2 strain or variant in a susceptible cell line : evaluation of the susceptibility of a cell line, evaluation of the infectivity of a variant compared to a reference variant, evaluation of the effect of infection on a cellular pathway etc... The project can be refined upon request

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the NTD & RBD (nt 1 to 1572 in the spike coding sequence) of the SARS-CoV-2 alpha variant (B.1.1.7) 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.

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the NTD & RBD (nt 1 to 1517 in the spike coding sequence) of the SARS-CoV-2 beta variant (B.1.351 )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.

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the NTD & RBD (nt 1 to 1581 in the spike coding sequence) of the SARS-CoV-2 BavPat1 strain (D614G) 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.

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the NTD & RBD (nt 1 to 1581 in the spike coding sequence) of the SARS-CoV-2 delta variant (B.1.617.2) 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.

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.

RNA extracted from infected cell culture supernatant of Pirital virus. Virus Provenance: Venezuela

RNA extracted from infected cell culture supernatant of Parana virus, Paraguay, 1966

RNA extracted from infected cell culture supernatant of Tacaribe virus