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.
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.
Murine monoclonal antibody, clone 2D2A3, directed against a ~60 kDa protein of Kamiti river virus (NS3?). It do not cross-react with Hanko virus and works in immunofluorescence test and WB.
Murine monoclonal antibody, clone 4F11A2, directed against a ~40 kDa protein (NS1?) of Hanko virus. It do cross-react with Kamiti River virus and works in immunofluorescence test and in WB.
Murine monoclonal antibody, clone 4C3A1B, directed against a ~70 kDa protein (NS3?) of Hanko virus. It do not cross-react with Kamiti River virus and works in immunofluorescence test and only weakly in WB.
Linear peptide epitopes within the SARS-CoV-2 envelope protein (#1: aa 44-55, #2: aa 59-72). The peptides are fused to a multimeric protein scaffold based on Lumazine Synthase. The particles were expressed in E.coli and purified by FLAG-affinity chromatography.
Unit: 500 µg of one peptide or 250 µg of both peptides
Carnation Italian ringspot virus full-length cDNA cloned in plasmid pUC18, under the control of a T7 promoter, allowing for transcription of infectious RNA
Unit: 2 micrograms plasmid DNA, allowing for the inoculation of six host plants (Nicotiana benthamiana) after T7-driven transcription
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