Semliki forest virus original isolate. This Semliki forest virus is freeze dried.Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
Tick-borne encephalitis virus, strain Hypr original isolate. This Tick-borne encephalitis virus[Hypr] is freeze dried.Tests for the presence of mycoplasmae were negative.
Chikungunya virus, strain Ross original isolate. This Chikungunya virus[Ross] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
Eastern equine encephalitis virus original isolate. This Eastern equine encephalitis virus[EEE 2090-EEE 2090] is freeze dried. Tests for the presence of mycoplasmae were negative.
Hantaan virus. This Hantaan virus[76-118] 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.
Tick-borne encephalitis virus, strain RSSE (Far eastern subspecies) original isolate. This Tick-borne encephalitis virus[RSSE] is preserved under Freeze Dried (-20C).Tests for the presence of mycoplasmae were negative.
Unit: 2 vials of freeze dried material to be resuspended in 0,25 ml
West Nile virus original isolate. This West Nile virus is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
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.
Tula virus [Moravia/5302Ma/94] cDNA to be used as a positive control for PCR. Total RNA prepared from cell culture supernatant and transcribed using random hexamers.
DOBV Slovakia/Aa cDNA to be used as a positive control for PCR. Total RNA prepared from cell culture supernatant and transcribed using random hexamers.
