EVAg

Freeze-dried human plasma spiked with heat inactivated Mayaro virus culture supernatant, (non infectious)

Diagnostic systems and positive controls for arboviruses containing : 960 tests for Dengue virus detection, 960 tests for Chikungunya virus detection 960 tests for Zika virus detection For Research use only

In an outbreak situation in crops, it is necessary to obtain quickly a good overview of the viruses that may be involved. Only in this way can the right measures be taken to safeguard crop production immediately but also in the long term. High-throughput sequencing (HTS) and bioinformatics analysis of samples offer a global analysis of the phytosanitary status of plants and the rapid and precise identification of pathogens.

Purified plasmids with: S segment of Mopeia virus, L segment of Mopeia Virus, NP Expression plasmid, L expression plasmid, all under T7 Polymerase promotor; 100 ng per Plasmid, shipped at RT. Rescue of virus requires cell line expressing T7 Polymease (e.g. BSR-T7 cells) or co-transfection of a T7 polymerase plasmid; cells are not included in this bundle

Plasmid coding the full-length antigenome of Ebola virus isolate Makona from West African outbreak 2014. The plasmid can be used for the rescue of recombinat virus.

Plasmid coding the full-length antigenome of Ebola virus Zaire isolate Mayinga (AF086833) . The plasmid can be used for the rescue of recombinat virus.

Plasmid encoding the full-length anti-genome of Marburg virus strain Musoke under the control of the T7 polymerase for rescue experiments. The plasmid contains two genetic markers: insertion of a SacII restriction site in the GP gene (nt position 10511a to g silent mutation) and a silent mutation at nt position 9485 c toT in the GP gene resulting in the deletion of a KpnI restriction site

Freeze-dried human plasma spiked with heat inactivated West Nile virus culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Tick borne encephalitis virus culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Zika virus culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated chikungunya virus culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Dengue virus 4 culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Dengue virus 3 culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Dengue virus 2 culture supernatant, (non infectious)

Freeze-dried human plasma spiked with heat inactivated Dengue virus 1 culture supernatant, (non infectious)

RNA extracted from infected tissue, Oropouche virus (RIVM/OROV/TRVL9760/09/11/1967).

During visit of the facility examples for comprehensive detection and measures to control quarantine pathogens (viruses, bacteria, fungi, nematodes) will be presented and the associated quality management will be demonstrated. Furthermore time for mutual scientific exchange and discussions on the control of known and emerging viruses is given. The number of applicants is limited to one to two persons per visiting period.

Full length Hendra virus genome clone to produce recombinant virus

Full length Nipah virus Bangladesh genome clone to produce recombinant virus

*2 SPOTS ONLY REMAINING* An in-depth theoretical and practical application of biosafety, biocontainment and biosecurity under the Australia/New Zealand standards and Australian regulatory framework for Biosecurity Containment and Physical Containment level 3 and 4 laboratory and animal facilities.

Purified recombinant NS1 protein (C-terminal His-Tagged) expressed in mammalian HEK293F cells as secreted protein

Porcine Reproductive and Respiratory Syndrome Virus (PRRSV-1) RNA. PRRSV-1 risk group is unclassified and is for the recipient lab to perform their own risk assessment and handle it accordingly.

WEN3; LCMV-WE GP neutralizing antibody, monoclonal antibody, mouse IgG2a

Galinsoga mosaic virus full-length cDNA is cloned in plasmid pUC18, under the control of a T7 promoter, allowing for transcription of infectious RNA

Tomato bushy stunt virus full-length cDNA is cloned in plasmid pUC18, under the control of a T7 promoter, allowing for transcription of infectious RNA