EVA

RNA extracted from infected cell culture supernatant of Cupixi virus, Brazil

Freeze-dried Mammalian orthoreovirus 4, strain Ndelle v. Cameroon, complete ORF sequence.

RNA extracted from infected cell culture supernatant.

Freeze-dried Mammalian orthoreovirus 3, strain Dearing 824-VR, partial sequence.

Freeze dried West Nile virus, strain UVE/WNV/UNK/EG/Egypt 101, Egypt, partial sequence.

RNA extracted from infected cell culture supernatant. Virus Provenance: St Martin, French Caribbean

Plasmid for quantification in the real-time RT-PCR assay (Hofmann et al. 2008)

LCMV Clone 13 expressing the glycoprotein of strain WE and carrying a mutation N63K to convert the GP61-80 CD4 epitope to the sequence of the Armstrong/Clone strain and, additionally, carrying a glycoprotein Y72F mutatio

LCMV Clone 13 expressing the glycoprotein of strain WE and carrying a mutation N63K to convert the GP61-80 CD4 epitope to the sequence of the Armstrong/Clone strain and, additionally, carrying a glycoprotein V71S mutatio

LCMV Armstrong expressing the glycoprotein of strain WE and carrying a mutation N63K to convert the GP61-80 CD4 epitope to the sequence of the Armstrong/Clone strain and, additionally, carrying a glycoprotein V71S mutati

LCMV Clone 13 expressing the glycoprotein of strain WE and carrying a mutation N63K to convert the GP61-80 CD4 epitope to the sequence of the Armstrong/Clone strain

LCMV Armstrong expressing the glycoprotein of strain WE and carrying a mutation N63K to convert the GP61-80 CD4 epitope to the sequence of the Armstrong/Clone strain

anti-Zaire ebolavirus (EBOV-Zaire) VP30

Rabbit polyclonal antiserum raised against BPL inactivated West Caucasian bat lyssavirus. The antiserum has been shown to specifically neutralize West Caucasian bat lyssavirus.

RNA from West Caucasian bat lyssavirus, RV3384, in HPLC water. The RNA was extracted from virus cultured in BHK-21 cell using Trizol LS.

Access to AMU/AFMB infrastructure for learning/training on techniques related to viral recombinant proteins

Training in Coronavirus reverse genetics to adapt novel techniques (ISA method) to large RNA viruses and compare different technologies under BSL-3 conditions

Lyophilized encapsidated RNA for SARS-CoV-2 (2019-nCoV) real time RT-PCR targeting region of the RdRp (IP2/IP4) gene, for 100 Rxns (Target designed by Institut Pasteur: https://www.who.int/docs/default-source/coronaviruse/real-time-rt-pcr-assays-for-the-detection-of-sars-cov-2-institut-pasteur-paris.pdf?sfvrsn=3662fcb6_2) 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)

A bundle of rodent-borne virus stocks to be used for EQA preparation

Expression plasmids for the production of flaviviruses NS5 full length (MTase and RdRp domains). Synthetic gene optimized for E. coli. Coding sequence fused at its 5' with a cleavage 6His tag coding sequence

The in vitro transcribed RNA is the control for the first-line screening assay termed E gene assay. The SARS-CoV full virus RNA is required to control the two confirmatory assays. Dislaimer: Import permit maybe be needed in your country for the SARS-CoV full virus RNA. If yes, please indicate so in your online enquiry.

Lyophilized encapsidated RNA for SARS-CoV-2 (2019-nCoV) real time RT-PCR targeting region of the RdRp gene, for 25 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)

anti-Gn or Gc protein of Tula orthohantavirus, clone 4G10A3, cell culture supernatant

Lyophilized encapsidated RNA for SARS-CoV-2 (2019-nCoV) real time RT-PCR targeting region of the E gene, for 100 Rxns (Target designed by Charité Universitätsmedizin Berlin ; https://www.who.int/docs/default-source/coronaviruse/wuhan-virus-assay-v1991527e5122341d99287a1b17c111902.pdf). 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)

IF-slides to detect anti-nCoV antibodies by Immunofluorescence assay. The slides were prepared by infecting Vero cells with the first Swedish SARS-CoV-2 isolate (SARS-CoV-2/01/human/2020/SWE). The virus is fully sequenced (Genebank accession: MT093571). The slides are fixated in acetone, air-dried and preserved at -80°C. IF-analysis tested positive with SARS-CoV-2 infected human sera.