Genetic modification is a prerequisite for today's target research and cell based assay screening for compound development. Viral vectors work both in vitro and in vivo, are versatile and warrant high gene delivery rates: The viruses' own infection machinery is being used to transport genetic material into the host cells. Several viral vector platforms are in use: lentivirus lends itself to sta-ble gene modifications as opposed to transient modifications like with adenovirus (AV) and adeno-associated virus (AAV).
Specialized service providers like SIRION Biotech are able to provide custom lentivirus and the resulting stable cell pools within a matter of weeks, premade lentiviral particles can be shipped literally over night. The availability of such focused services allows for faster and more reliable research. Viral vector technologies are applicable from drug discovery to food sciences and cosmetics developments.