EVAg

Entry Plasmid of CoVOC43 Nsp5, Full gene(cTLpro), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp5, Full gene (cTLpro), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp16, Full gene (2'O MTase), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp10, Full gene (UNK), in fusion with a C-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp10, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp8, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp7, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp16, Full gene (2'o MTase), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp15, Full gene (NendoU), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of CoVOC43 Nsp13, Full gene (Zc+HEL), in fusion with a N-Terminal His tag coding sequence

Coding sequence of 2C protein from Coxsackie B3 virus cloned in pMCOX20a with his/TRX tag coding sequence in 5’. For recombinant expression of the protein in E.coli. The 116 Nterminal amino acids of 2C protein have been removed and the his/TRX tags are removable with TEV protease.

Expression clone for the Tha virusViral polymerase (Large protein, L) from Tha rabies virus

Complete cDNA of Th4M genome cloned in pSDI-HH-flash-SC vector

Complete cDNA of Th2P4M genome cloned in pSDI-HH-flash-SC vector

Complete cDNA of Th2P genome cloned in pSDI-HH-flash-SC vector

Complete cDNA of Tha genome in pSDI-HH-flash-SC vector

Expression clone for the Tha virus Nucleoprotein

Expression clone for the Tha virus Phosphoprotein

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

Plasmid for in vitro transcription that contains the 5`UTR region of an Aichi virus for 5`UTR-Leader region PCR assays published by Drexler et al, Emerg Infect Dis. 2011

Human Coronavirus 229E plasmid for in vitro transcription.

Double-stranded DNA copy of a coxsackievirus A17 genome without the capsid-encoding region, cloned into a plasmid backbone downstream a T7 promoter. After in vitro transcription, the corresponding RNA can be transfected into cells to give rise to a replicon that is self-replicative and can express the non-structural virus proteins but is unable to produce infectious particles. The plasmid can be amplified in E. coli.

Infectious clone: double-stranded DNA copy of the genome of Coxsackievirus A17 strain 67591 downstream a T7 promoter in a plasmid backbone. In vitro transcribed RNA produces the virus upon transfection of permissive cells. The plasmid can be amplified in E. coli.

Grapevine pinot gris virus, isolate SK30. Complete genome sequence cloned in pCass2 vector.

Reverse genetics-based life cycle modelling system that allows modelling of Ebola virus genome replication and transcription, viral protein synthesis, virus assembly, budding, and entry into target cells under BSL1 conditions.