I was just wondering if one could resuspend the lentivirus pellet in whatever culture medium, instead of PBS. In this way maybe the final concentration of virus can get higher when later transducing cells?
Actually, It is our routine to concentrate supernatant containing viruses and then remaining viruses with little media would be used to transduce the target cells. It is the best if you remove the equal volume from the media of cells and use media containing viruses for trasnduction.
It depends on what you planning to do with the virus, it will be no problem to resuspend them in the chosen media for transduction of what ever cell culture you chose. We resuspend our in PBS as we would do animal works with the virus, so media would'nt be recommended.
Hey just to clarify things better, when you guys suspend virus in medium and freeze the aliquots, your medium contains FBS and L-glutamine, right? Or just medium without adding anything?
Yes, in our method, media is complete and we keep media containing virus in 4 degree for a few days until collecting media containing virus is done and then use it for transduction. Freezing and thawing again of viruses decrease virus transduction efficiency.
A Mostafa mentioned, you can keep in complete media at 4 degree for not more than 1 week, or you'll see decrease in you virus titer, even storing at -80 you'll see decrease in virus titre with time. Key point is make fresh, store in small aliquots.