EVAg

HCV X-tail Plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

Invitro transcript for Hepatitis C virus genomic x-tail region assays.

In vitro transcribed RNA for HCV real time PCR.

HCV 5`ncr Plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

Invitro transcript for Hepatitis C virus genomic 5`ncr region assays. 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.

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

Dengue virus serotype 3 plasmid for in vitro transcription. The target region of a specific real time assay was amplified and cloned.

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

Dengue virus serotype 1 plasmid for invitro transcription - Target region of a specific real time assay was amplified and cloned.

Dengue virus serotype 1 RNA extracted from infected cell culture lysate.

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

Viral RNA extracted from infected cell culture lysate.

in vitro transcribed RNA for a specific Yellow fever virus real time PCR

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

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, 638-727 Insert Sequence: 37-637

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 and in vitro transcribed. In vitro transcript: Vector Sequence: Position 1-36, 727-816 Insert Sequence: Position 37-726

Yellow fever virus 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 (positive control) for a Usutu virus real time PCR. (Ref: J Virol Methods. 2014 Mar;197:51-4. doi: 10.1016/j.jviromet.2013.08.039. Epub 2013 Sep 13, "Development of a Usutu virus specific real-time reverse transcription PCR assay based on sequenced strains from Africa and Europe." Nikolay B1, Weidmann M2, Dupressoir A3, Faye O4, Boye CS5, Diallo M6, Sall AA7.)

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.

17 freeze dryed inactivated samples in screw cap tubes

BPL inactivated cell culture supernatant