“…Because the integration and the expression of retroviral constructs requires mitotic division of the target cells, we first culture the quiescent CB cells, for 24 hours in presence of Stem Cell Factor (SCF), Trombopoietin (TPO), Flt ligand 3 (FLT-3) and Interleukin 6 (IL-6)(Akkina et al, 1996). Then, the cells were seeded over retronectin-coated plates previously pre-adsorbed with the viral particles, as previously described (Gammaitoni et al, 2006). Using this approach, we obtained an infection efficiency of approximately 28% as monitored by a constitutive GFP reporter retrovirus.…”