Bundle of freeze-dried tick-borne encephalitis virus (TBEV) isolates representing the diversity of the virus in Central Europe and covering various isolation sources (tick, rodent, milk).
We offer a 5 day training session to colleagues from endemic regions. Participants will visit the Viroscience clinical virology lab, where they will perform all required laboratory and analysis procedures for the quantification rabies virus and neutralizing antibodies.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[A104] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
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.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[114] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[114] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis[Clg223] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis[Clg223] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[285] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been partly sequenced.
TBEV isolate from our collection (IVSAS). This Tick-borne encephalitis virus[285] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative.
P1 cultured virus from a monkey pox positive patient.
First Dutch isolate from MPXV infected patient.
NOTE: This material is not available for commercial purposes, such as contract research services”
Training in reverse genetics method (ISA method), recently developed to reconstitute an infectious Flavivirus or Alphavirus under BSL-3 conditions.
The training comprises DNA fragments amplification by PCR; Transfection of the purified products into permissive cells; Viral culture; Molecular detection
Infectious cell culture supernatant. This virus is preserved under Viral Storage Medium -80C. The cell culture used to replicate this virus was confirmed mycoplasm free.
Infectious cell culture lysate. This Yellow fever virus[17D vaccine] is preserved under Viral Storage Medium -80C. To confirm its identity the virus has been fully sequenced.
Infectious cell culture lysate. This West Nile virus[Egypt 101] is preserved under Viral Storage Medium -80C. Virus is mycoplasma free. To confirm its identity the virus has been fully sequenced.
Infectious cell culture lysate. This Japanese encephalitis virus [strain Nakayama] is freeze dried. Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been fully sequenced.
Infectious cell culture supernatant. This virus is preserved under Viral Storage Medium -80C. The cell culture used to replicate this virus was confirmed mycoplasm free.
Infectious cell culture lysate. This Japanese encephalitis virus[Nakayama] is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were positive.
This West Nile virus strain is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been fully sequenced.
This West Nile virus strain is preserved under Viral Storage Medium -80C.Tests for the presence of mycoplasmae were negative. To confirm its identity the virus has been fully sequenced.
