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In many studies, viral vectors have become the preferred method of delivery. Adenovirus is by far the most effective gene delivery vector, with nearly 100% efficiency against both dividing and non-dividing mammalian cells. Therefore, more efficient gene silencing can be achieved with adenovirus or AAV systems compared to other methods (direct transfection of siRNA/plasmid, retrovirus, and lentiviral systems). shRNA Adenovirus https://integraterna.creative-....biogene.com/service/