Hello there! I have some query to solve regarding my lentivirus infection! I have successfuly generated lentivirus particles by 293T transfection. And i have used this supernatent to infect 293T cells, but i am unable to get clear GFP signal (marker). so my questions are; 1: what is the best way to cencentrate lentivirus? can i use centricon (if yes what's the optimal pore size? 2:how to increase infection efficiency? is there some reagent i can use which is compatible to 293T cells?