EVAg

In vitro transcribed RNA for a specific JEV (Japanese encephalitis virus) real time PCR, here: NS2A (Ref: Article Source: Development of an improved RT-qPCR Assay for detection of Japanese encephalitis virus (JEV) RNA including a systematic review and comprehensive comparison with published methods Bharucha T, Sengvilaipaseuth O, Vongsouvath M, Vongsouvath M, Davong V, et al. (2018) Development of an improved RT-qPCR Assay for detection of Japanese encephalitis virus (JEV) RNA including a systematic review and comprehensive comparison with published methods. PLOS ONE 13(3): e0194412.

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.

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

West Nile virus original isolate. This West Nile virus[Ntaya virus group.] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.

Louping ill virus original isolate. This Louping ill virus[Louping ill] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.

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,

Negishi virus - original isolate. This Negishi virus is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.

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.

Freeze-dried Tick Borne Encephalitis Virus, strain UVE/TBEV/2013/FR/32.11 WT-PCR, complete ORF sequence. It was produced by ISA method from infectious clone derived from Oshima 5.10 strain (genbank sequence KF623542)

Freeze-dried Tick-borne encephalitis virus, strain UVE/TBEV/2013/FR/32.11 ɸNS5-PCR, partial sequence.

Freeze-dried Tick-borne encephalitis virus, strain UVE/TBEV/2013/FR/32.11 ɸNS3 ɸNS5-PCR, complete ORF sequence.

Kyasanur forest disease virus - original isolate. This Kyasanur forest disease virus[KFD] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.

Tick-borne encephalitis virus, strain RSSE (Far eastern subspecies) original isolate.

TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[A104] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.

Freeze-dried Turkish sheep encephalomyelitis virus strain UVE/TSEV/UNK/TR/TTE80, Turkey, complete ORF sequence.

Tick-borne encephalitis virus, strain Hypr original isolate. This Tick-borne encephalitis virus[Hypr] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.

West Nile virus original isolate. This West Nile virus is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.

Japanese encephalitis virus - original isolate. This Japanese encephalitis virus[Japanese encephalitis] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.