Description
Lentiviral expression vectors are one of the most effective vehicles to introduce and stably express different effector molecules (siRNA, cDNA, DNA fragments, antisense, ribozymes, etc.) or reporter constructs into almost any mammalian cell, including non-dividing cells and whole model organisms. Lentiviral vectors integrate into the host cell genome and are passed onto daughter cells --Cells can be treated, grown for several passages, frozen and thawed the lentiviral construct remain in the host cells --Vector contains fluorescent marker and antibiotic selection to ensure stability