EVAg

plasmid encoding the VSV antigenome, lacking the G gene, and encoding mCherry, for producing recombinant VSV lacking a glycoprotein for pseudotyping assays or for cloning and production of VSV encoding foreign glycoproteins.

plasmid encoding the VSV antigenome with an additional transcription unit encoding mCherry for production of recombinant VSV expressing mCherry

pCMV-Nopt: codon-optimized plasmid expressing the VSV Indiana N protein

pCMV-Popt: codon-optimized plasmid expressing the VSV Indiana P protein

plasmid encoding a codon-optimized VSV L gene for recovery of recombinant VSV

plasmid encoding the VSV antigenome, lacking the G gene, and encoding eGFP, for producing recombinant VSV lacking a glycoprotein for pseudotyping assays or for cloning and production of VSV encoding foreign glycoproteins.

Training in reverse genetics method (ISA method), recently developed to reconstitute an infectious Flavivirus or Alphavirus under BSL-3 conditions. The training comprises DNA fragments amplification by PCR; Transfection of the purified products into permissive cells; Viral culture; Molecular detection

Aeonium ringspot virus, RNA1 and RNA2 full-length cDNAs are cloned in plasmid pUC18, under the control of a T7 promoter, allowing for transcription of infectious RNAs.

The 3' terminal 217 nts of Aeonium ringspot virus RNA1 and RNA2 (excluding the poly(A) tail) are cloned in pGEM-T Easy allowing for transcription of a riboprobe to detect both genomic RNAs.

12 freeze dryed inactivated samples in screw cap tubes

Neuraminidase subtype N2 (amino acids 30 - 461) from Influenza A virus subtype H9N2 (A/Bat/Egypt/381OP/2017). The protein is equipped with a c-terminal FLAG-tag and was expressed in Expi293 cells. Purification was performed using FLAG-M2 affinity chromatography followed by dialysis against 1X PBS pH 7.4.

Viral RNA extracted from infected cell culture lysate.

Human parainfluenzavirus 1 plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

Herpes simplex virus Plasmid for real time PCR. The target region of a specific real time assay was amplified and cloned.

Human parainfluenza virus 4 plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

Plasmid for JC virus real time PCR. The target region of a specific real time assay was amplified and cloned.

Human parainfluenza virus 3

Target region of a specific real time assay was amplified and cloned.

Human Adenovirus plasmid for real time PCR. The target region of a specific real time assay was amplified and cloned.

Human parainfluenza virus 2 plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

Target region of a specific real time assay was amplified and cloned.

in vitro transcribed RNA for a specific Sapovirus real time PCR.

Plasmid for a specific human parvovirus B19 real time PCR. The target region of a specific real time assay was amplified and cloned.

Human respiratory syncytial virus plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

in vitro transcribed RNA for a specific human parainfluenza virus 2 real time PCR.