Primary neural stem cells (NSCs) can be cultivated and differentiated in vitro
but are difficult to transfect using conventional methods. We describe a simple and rapid magnetofection-based method suitable for the lab bench as
well as high-throughput projects. Our method yields high transfection efficiency and can be used for deciphering the genetic control of neural cell
differentiation.
but are difficult to transfect using conventional methods. We describe a simple and rapid magnetofection-based method suitable for the lab bench as
well as high-throughput projects. Our method yields high transfection efficiency and can be used for deciphering the genetic control of neural cell
differentiation.
No comments:
Post a Comment