https://www.selleckchem.com/pr....oducts/cenicriviroc.
Produced cells contain 60% CAR+ cells with VCN less then 3. In summary, the described manufacturing platform enables a straightforward cGMP certification, since the transposon and transposase are produced abiotically in vitro via enzymatic synthesis. It is suitable for the cost-effective production of highly experimental, early-phase CAR T cell products.Hepatic gene transfer with adeno-associated viral (AAV) vectors shows much promise for the treatment of the X-linked bleeding disorder hemophilia B in multiple clinical trials.
Мне нравится
Комментарий
Перепост
