This page lists the EVAg products having been related to the "Zika virus"
taxonomic term. The additional filters enable you with creating a sub-selection of items of
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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.
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
A specific RT-PCR was performed on KJ776791. The product was cloned into a vector, sequenced and in vitro transcribed. In vitro transcript: Vector Sequence: Position 1-36, 727-816 Insert Sequence: Position 37-726
A specific genome region was amplified by PCR, cloned into a vector and in vitro transcribed. In vitro transcript: Vector Sequence: 1-36, 632-721 Insert Sequence: 37-631
A specific RT-PCR was performed on KJ776791. The product was cloned into a vector, sequenced an in vitro transcribed. In vitro transcript: Vector Sequence: 1-36, 638-727 Insert Sequence: 37-637
A specific RT-PCR was performed on KJ776791. The product was cloned into a vector, sequenced an in vitro transcribed. In vitro transcript: Vector Sequence: 1-36, 674-763 Insert Sequence: 37-673
A specific RT-PCR was performed on KJ776791. The product was cloned into a vector, sequenced an in vitro transcribed. In vitro transcript: Vector Sequence: 1-36, 634-723 Insert Sequence: 37-633
Pure recombinant protein for enzymatic assay and structural studies. MTase domain including amino acid 1 to 264 of ZIKV NS5, with a N-terminal 6-His tag.
Expression plasmid for the production of the Nterminal - Domain of ZIKV NS5 (methyltransferase domain). Synthetic gene optimized for E. coli. Coding sequence fused at its 5' with a 6His tag coding sequence
Expression plasmid for the production of the Nterminal - Domain of ZIKV NS5 (methyltransferase domain, amino acids 4-278). Synthetic gene optimized for E. coli. Coding sequence fused at its 5' with a 6His tag coding sequence
Quantified freeze-dried genomic standard for molecular detection of Zika virus, made of an inactivated culture supernatant of strain H/PF/2013 (full sequence of the virus strain KJ776791.1) with quantified genomic titre.
Quantified freeze-dried genomic standard for molecular detection of Zika virus, made of an inactivated culture supernatant of strain MRS_OPY_Martinique_PaRi_2015 (full sequence of the virus strain KU647676.1) with quantified genomic titre.
