EVAg

In vitro transcribed RNA (positive control) for a Usutu virus real time PCR. (Ref: J Virol Methods. 2014 Mar;197:51-4. doi: 10.1016/j.jviromet.2013.08.039. Epub 2013 Sep 13, "Development of a Usutu virus specific real-time reverse transcription PCR assay based on sequenced strains from Africa and Europe." Nikolay B1, Weidmann M2, Dupressoir A3, Faye O4, Boye CS5, Diallo M6, Sall AA7.)

Monkeypox 2022 outbreak strain

DNA extracted from clarified supernatant from infected cell culture.

DNA extracted from clarified supernatant from infected cell culture.

DNA extracted from clarified supernatant from infected cell culture.

X-ray inactivated SARS CoV2 Omicron B.1.1.529.BA.2

Inactivated SARS CoV2 Omicron B.1.1.529.BA.2

Recombinant NS1 from Dengue virus serotype 3, produced in Expi293F HEK cells, fused to an Hexahistidine tag.

Production on request of stabilisated RNA positif control, as known as Armored RNA for RT-PCR. This service includes: - Design of the positif control sequence based on the sequence provided by the costumer - Production and lyophilisation of Armored RNA according the quantity needed - LOD/quantification - Shipment of the Armored RNA at room temperature

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

The lyophilized, non infectious, encapsidated RNA (Armored RNA) contains the sequence of the 3'UTR and the pro-Capside region from West Nile virus 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.

BPL inactivated cell culture supernatant

BPL inactivated cell culture supernatant

Recombinant hemagglutinin-esterase of Bovine coronavirus strain L9 (amino acids 17 - 392). The protein was expressed in Expi293 cells and Streptactin-purified. It is equipped with a c-terminal SpyTag (RGVPHIVMVDAYKRYK) and a single StrepTag

Recombinant receptor binding domain of Bovine coronavirus strain L9 (amino acids 311 - 695 of the Spike protein) . The protein was expressed in Expi293 cells and Streptactin-purified. It is equipped with a c-terminal SpyTag (RGVPHIVMVDAYKRYK) and a single StrepTag

E2 glycoprotein of the Norway rat pestivirus isolate NrPV/NYC-D23; amino acids 803 - 1150 of the polyprotein. C-terminally, a single StrepTag was added. The protein was expressed in Expi293 cells and purified by Streptactin affinity chromatography.

Lyophilized ready-to-use primers and probe (Lyoph-P&P, 180 rxns in the form of 10x18 rxns) for real time RT-PCR of Multiplex Dengue Serotyping (Taqman) SOPs in the attached pdf. Disclaimer: This product does not contain the polymerase. For RUO (research use only).

anti-SARS-CoV-2 NSP 1 monoclonal antibody, clone 5F10C2

anti-SARS-CoV-2 NSP 1 monoclonal antibody, clone 4D10A2B

freezed dried and inactivated variants of HCoV and SARS

freezed dried and inactivated Omicron subtypes

Freeze-dried human plasma spiked with heat inactivated Dengue virus 3 (strain 2015/TH/7716) culture supernatant, (non infectious)

Murine monoclonal antibodies, clone 1D10A3, directed against an unknown protein of Toscana phlebovirus. It do not cross-react with Salehabad phlebovirus and Naples phlebovirus and works in immunofluorescence test only.

Murine monoclonal antibodies, clone 8F2A1, directed against the N protein of Toscana phlebovirus. It do not cross-react with Salehabad phlebovirus and Naples phlebovirus and works in immunofluorescence test and WB.

Murine monoclonal antibodies, clone 2F2B2, directed against the N protein of Salehabad phlebovirus. It do not cross-react with Toscana phlebovirus and Naples phlebovirus and works in immunofluorescence test and WB.