EVAg

Langat virus cDNA

Langat virus RNA

Tahyna virus cDNA to be used as a positive control for PCR. Total RNA prepared from cell culture supernatant and transcribed using random hexamers.

Tahyna virus RNA

Tribec virus RNA

Anti-Rift Valley Fever Virus; RVFV; NSs reference constisting of 6 different antibodies

Viral RNA from laboratory Zika strain MP1751 infected veros,

VSV-IND-neutralizing antibody

Infectious Subgenomic Amplicons Reverse genetic system for chimeric virus CH-17D / ZIKV. It consists of three non infectious overlapping DNA fragments (cloned into pUC57 vector) . These products enable to obtain infectious RNA virus after amplification by PCR, and transfection into susceptible cells. The chimeric virus systems were constructed using the yellow fever 17-D vaccine strain as a genetic backbone and by replacing prM/E from this vaccine strain with those of the Asian ZIKV PF epidemic strain.

Hybridoma cell culture supernatant containing anti-Influenza A virus antibodies; targeted antigen: Matrix Protein 1; clone: 4.2.1.A; immunization antigen: several inactivated AIV HxN2 isolates

Plasmid for expression of the LCMV Armstrong strain L-segment in rodent cells; [also termed pI-L-ARM(-) or pDP067]

Expression plasmid of the LCMV strain clone 13 "S" segment expressing WE glycoprotein [also termed pol-I-S-WE(-) or pDP009]

Plasmid for the expression of the LCMV strain Armstrong L-protein in eukaryotic cells. [also termed pC-L_ARM-BsmB pDP062]

Expression plasmid of the LCMV strain Armstrong S segment in rodent cells [also termed polI-S-ARM or pDP073]

This five-day course includes two modules that can be attended separately. In the first module (Ref-SKU: 011S-02851), the basic principles of routine virus typing that can be used for hospital epidemiology and public health will be addressed by a combination of lectures, demonstration and hands-on training. Participants will visit the Viroscience clinical virology lab, where they will perform all required laboratory and analysis procedures for routine typing of viruses.

This five-day course includes two modules that can be attended separately. In the first module (Ref-SKU: 011S-02851), the basic principles of routine virus typing that can be used for hospital epidemiology and public health will be addressed by a combination of lectures, demonstration and hands-on training. Participants will visit the Viroscience clinical virology lab, where they will perform all required laboratory and analysis procedures for routine typing of viruses.

Recombinant 3C protease of Coxsackie B3 virus. Produced in E. coli, purified in non denaturing conditions. Suitable for protein crystallization, functional assays, or tag cleavage.

Hybridoma cell culture supernatant containing anti-CCHFV antibodies; targeted antigen: glykoprotein Gn/Gc; clone: 4H12B3; immunization antigen: recombinant Gn/Gc protein, strain "IbAr 10200"

Hybridoma cell culture supernatant containing anti-SPDV antibodies; targeted antigen: unknown; clone: 15B8; immunization antigen: inactivated strain "S49P (rainbow trout)"

Hybridoma cell culture supernatant containing anti-SPDV antibodies; targeted antigen: envelope; clone: 12A5; immunization antigen: inactivated strain "S49P (rainbow trout)"

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.

In this 1 week course the basic principles of methods used to conduct phylogenetic analysis of enterovirus genomes will be addressed by a combination of lectures, demonstration and hands-on training. Participants will perform all required analysis procedures using different bioinformatics tools. Topics included: Selection of genomic regions used for phylogenetic analysis – Selection of relevant sequences in public database to be included in the analysis – Search for recombination events

This course constitutes an optional week that can supplement the course « Isolation of enteroviruses from clinical samples – Detection by real-time RT-PCR ». This training will focus on methods used to perform titration of enterovirus stock solutions and to conduct enterovirus purification by plaque assays.