EVAg

cDNA of Zika virus isolate Brazil/2016/INMI1, obtained from reverse transcription with non specific hexamers primers. The cDNA was obtained from a Brasilian viral strain isolated in Italy, from a sample collected in January 28, 2016.

RNA of Human 2019-nCoV strain 2019-nCoV/Italy-INMI1. The RNA was obtained from a viral strain isolated in Italy, from a sample collected in January 29, 2020. To confirm its identity the virus has been completely sequenced. The complete sequence was submitted to GenBank (SARS-CoV-2/INMI1-Isolate/2020/Italy: MT066156) and is available on GISAID website (BetaCoV/Italy/INMI1-isl/2020: EPI_ISL_410545) upon registration. Import permit can be needed in your country. If yes, please indicate it in your online enquiry.

WNV, strain 286.B/2013/Velky Biel/SVK, cDNA

WNV, strain 286.B/2013/Velky Biel/SVK, RNA

WNV, strain 200.B/2013/Secovce/SVK, RNA

WNV, strain 200.B/2013/Secovce/SVK, cDNA

This product represents total RNA extracted from the viral stock of SARS-CoV-2 strain Slovakia/SK-BMC5/2020 which is available as a viable virus under Ref-SKU: 006V-03933.

This product represents cDNA material, transcribed with random hexamers from total RNA extracted from the viral stock of SARS-CoV-2 strain Slovakia/SK-BMC5/2020 which is available as a viable virus under Ref-SKU: 006V-03933.

Infectious Subgenomic Amplicons Reverse Genetic system for Zika virus strain Dak84 (derived from genbank sequence KU955592). 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 cells,

Infectious Subgenomic Amplicons Reverse genetic system for Zika virus strain H/PF/2013. 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 cells,

Subgenomic Amplicons for Zika virus strain H/PF/2013. It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after transfection into cells.

Subgenomic Amplicons for Zika virus strain Dak84 (derived from genbank sequence KU955592). It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after transfection into cells

Subgenomic Amplicons for Japanese encephalitis virus strain CNS769_Laos_2009. It consists of three non infectious overlapping DNA fragments (amplicons). These products enable to obtain infectious RNA virus after transfection into cells

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.

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 OC43 plasmid for in vitro transcription

Human Coronavirus 229E plasmid for in vitro transcription.

in vitro transcribed RNA for Human coronavirus OC43 real time PCR

in vitro transcribed RNA for Human coronavirus 229E real time PCR

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

in vitro transcribed RNA for Human parechovirus real time PCR

Rhinovirus 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 Rhinovirus real time PCR.

Entry Plasmid of TGEV Nsp4, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence

Entry Plasmid of TGEV Nsp9, Full gene (UNK), in fusion with a N-Terminal His tag coding sequence