Hyperimmune polyclonal antiserum raised in a domestic pig challenged with Japanese encephalitis virus (JEV) Nakayama strain and boosted 47 days later. Serum was collected at day 83 post primary challenge.
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
The full-length genome of CpCDV (1.8 copies) is cloned in the binary plasmid vector pBin19, allowing transformation into Agrobacterium and infection of plants
Unit: 1 microgram, allowing infection of plants following transformation into Agrobacterium
Set of four controls of yellow fever genome (strain 17-D) for the verification of molecular detection assays. The samples have been calibrated against a molecular standard (ivRNA) of known genome copy number. The samples can be used as positive controls or as verification control for molecular assay performance. Product only available via TNA.
Unit: 1 set of four control samples of known copy number
Quantified freeze-dried genomic standard for molecular detection of Zika virus, made of an inactivated cell culture supernatant of strain MR766 with quantified genomic titre. Product only available via TNA.
Quantified freeze-dried genomic standard for molecular detection of yellow fever virus, prepared from an inactivated cell culture supernatant of strain YFV-17D with quantified genomic titre. Product only available via TNA.
The full-length genome of TYLCSV (1.8 copies) is cloned in the binary plasmid vector pBin19, allowing transformation into Agrobacterium and infection of plants
Unit: 1 microgram, allowing infection of plants following transformation into Agrobacterium
Protein A chromatography purified Mirafiori lettuce big vein virus (MiLBVV) polyclonal antibodies, raised in rabbit, suitable for serological detection
Viral RNA extracted from Bovine Viral Diarrhoea Virus type 1 (Isolate Ho916) grown in cell culture. The RNA is supplied in AVE buffer (Nuclease free water + 0.04% sodium azide).
Gp41 recombinant, carrying the "MIF" motif, typical for subtype AE, in the fusion domain of the subtype B prototype NL4-3 - for studying the fusion function.
Reverse genetics-based life cycle modelling system that allows modelling of Ebola virus genome replication and transcription, viral protein synthesis, virus assembly, budding, and Marburg virus entry into target cells under BSL1 conditions.
Quantified freeze-dried genomic standard for molecular detection of Yellow fever virus, made of an inactivated culture supernatant of Vaccinal strain 17D with quantified genomic titre.
In-house IF-slides to detect anti-CCHFV antibodies by Immunofluorecence assay. The slides were prepared by infecting Vero cells with the CCHFV strain, Nigerian IbAr10200. The slides are fixated in acetone, air-dried and preserved at -80°C. The slide has been tested positive with mouse monoclonal anti-CCHFV antibodies against N, Gc and Gn.