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- W2974396007 endingPage "72" @default.
- W2974396007 startingPage "49" @default.
- W2974396007 abstract "Transient gene expression (TGE)-based protein production in mammalian cells such as human embryonic kidney (HEK) 293 cells and Chinese hamster ovary (CHO) cells has been a valuable technology for the past two decades. Remarkable advances have been accomplished with regard to TGE-based platforms, with recombinant therapeutic protein titers increasing from mg/l to g/l. This development has primarily been spurred by an increased demand for screening multiple drug candidates in preclinical research. This improvement in TGE-based protein production is attributed to many factors: optimized transfection reagents, vectors with increased levels of gene expression, fit-for-purpose cell lines, cell line-specific serum-free media, and optimized cell culture processes for suspension cells. In this chapter, we outline how increase in foreign protein production using mammalian cell cultures has been achieved for TGE-based platforms with a focus on transfection methods, expression vectors, cell lines, and culture processes." @default.
- W2974396007 created "2019-09-26" @default.
- W2974396007 creator A5014571955 @default.
- W2974396007 creator A5017563610 @default.
- W2974396007 creator A5034018967 @default.
- W2974396007 creator A5051591184 @default.
- W2974396007 creator A5081619886 @default.
- W2974396007 date "2019-09-20" @default.
- W2974396007 modified "2023-10-16" @default.
- W2974396007 title "Transient Gene Expression‐Based Protein Production in Recombinant Mammalian Cells" @default.
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