Process analysis of reduced specific productivity of TNFR-Fc in Chinese hamster ovary cells at high cell density
暂无分享,去创建一个
Li Fan | Xu-ping Liu | W. Tan | Liang Zhao | Yan Zhou | Tianci Kou | Zhaoyang Ye
[1] Natarajan Vijayasankaran,et al. Understanding the intracellular effect of enhanced nutrient feeding toward high titer antibody production process , 2011, Biotechnology and bioengineering.
[2] Li Fan,et al. Effect of culture temperature on TNFR-Fc productivity in recombinant glutamine synthetase-chinese hamster ovary cells , 2010, Biotechnology Letters.
[3] Wei-Shou Hu,et al. Transcriptome and proteome analysis of Chinese hamster ovary cells under low temperature and butyrate treatment. , 2010, Journal of biotechnology.
[4] Li Fan,et al. Responses of GS-NS0 Myeloma cells to osmolality: Cell growth, intracellular mass metabolism, energy metabolism, and antibody production , 2009 .
[5] M. Butler,et al. Enhanced Production of Monomeric Interferon‐β by CHO Cells through the Control of Culture Conditions , 2008, Biotechnology progress.
[6] S. Gupta,et al. Effects of Elevated pCO2 and Osmolality on Growth of CHO Cells and Production of Antibody‐Fusion Protein B1: A Case Study , 2008, Biotechnology progress.
[7] H. Katinger,et al. Effect of Increased Expression of Protein Disulfide Isomerase and Heavy Chain Binding Protein on Antibody Secretion in a Recombinant CHO Cell Line , 2008, Biotechnology progress.
[8] S. Sharfstein,et al. Hyperosmotic Stress in Murine Hybridoma Cells: Effects on Antibody Transcription, Translation, Posttranslational Processing, and the Cell Cycle , 2008, Biotechnology progress.
[9] Sung Hyun Kim,et al. Effect of Low Culture Temperature on Specific Productivity and Transcription Level of Anti‐4–1BB Antibody in Recombinant Chinese Hamster Ovary Cells , 2008, Biotechnology progress.
[10] Yuanxing Zhang,et al. Gene transcription acceleration: main cause of hepatitis B surface antigen production improvement by dimethyl sulfoxide in the culture of Chinese hamster ovary cells , 2007, Biotechnology and bioengineering.
[11] J. Piret,et al. Decreased pCO2 accumulation by eliminating bicarbonate addition to high cell‐density cultures , 2007, Biotechnology and bioengineering.
[12] Wei-Shou Hu,et al. Fedbatch culture and dynamic nutrient feeding. , 2006, Advances in biochemical engineering/biotechnology.
[13] W. Miller,et al. Characterization of hybridoma cell responses to elevated pCO(2) and osmolality: intracellular pH, cell size, apoptosis, and metabolism. , 2002, Biotechnology and bioengineering.
[14] G. Lee,et al. Effect of hypoosmotic pressure on cell growth and antibody production in recombinant Chinese hamster ovary cell culture , 2001, Cytotechnology.
[15] M. Fussenegger,et al. A novel autoregulated proliferation-controlled production process using recombinant CHO cells. , 1999, Biotechnology and bioengineering.
[16] W. Miller,et al. Effects of CO2 and osmolality on hybridoma cells: growth, metabolism and monoclonal antibody production , 1998, Cytotechnology.
[17] J. Ljunggren,et al. Physiology of cultured animal cells. , 1997, Journal of biotechnology.
[18] M. Shuler,et al. Effect of elevated oxygen and glutamine levels on foreign protein production at high cell densities using the insect cell-baculovirus expression system. , 1997, Biotechnology and bioengineering.
[19] A. Zeng. Quantitative assessment of cell density effect on the metabolism and antibody production rate of hybridoma cells at high cell density , 1996 .
[20] ROGER C. Thomas. Bicarbonate briefly C02-free , 1995, Nature.
[21] C A Smith,et al. Soluble tumor necrosis factor (TNF) receptors are effective therapeutic agents in lethal endotoxemia and function simultaneously as both TNF carriers and TNF antagonists. , 1993, Journal of immunology.
[22] J. Bailey,et al. Effect of cloned gene dosage on cell growth and hepatitis B surface antigen synthesis and secretion in recombinant CHO cells , 1992, Biotechnology and bioengineering.
[23] M. Flickinger,et al. Use of a structured kinetic model of antibody synthesis and secretion for optimization of antibody production systems: I. Steady‐state analysis , 1992, Biotechnology and bioengineering.
[24] M. Flickinger,et al. A model of interorganelle monoclonal antibody transport and secretion in mouse hybridoma cells , 1991, Biotechnology and bioengineering.
[25] M. Flickinger,et al. A structured model for monoclonal antibody synthesis in exponentially growing and stationary phase hybridoma cells , 1991, Biotechnology and bioengineering.
[26] E. Mandine,et al. Evidence that monoclonal antibody production kinetics is related to the integral of the viable cells curve in batch systems , 1988, Biotechnology Letters.
[27] P. Chomczyński,et al. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.
[28] L. Goodman,et al. THE PHARMACOLOGICAL BASIS OF THERAPEUTICS , 1966 .
[29] G. Lee,et al. Effect of Akt overexpression on programmed cell death in antibody-producing Chinese hamster ovary cells. , 2009, Journal of biotechnology.
[30] M. Al‐Rubeai,et al. Detailed understanding of enhanced specific antibody productivity in NS0 myeloma cells , 2009, Biotechnology and bioengineering.
[31] Wei-Shou Hu,et al. Alteration of mammalian cell metabolism by dynamic nutrient feeding , 2004, Cytotechnology.
[32] Sigma S Mostafa,et al. Strategies for Improved dCO2 Removal in Large‐Scale Fed‐Batch Cultures , 2003, Biotechnology progress.
[33] G. Lee,et al. Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production , 2001, Biotechnology progress.
[34] M. Fussenegger,et al. Higher Productivity of Growth‐Arrested Chinese Hamster Ovary Cells Expressing the Cyclin‐Dependent Kinase Inhibitor p27 , 1998, Biotechnology progress.
[35] J. Lehmann,et al. Sialidase Activity in Culture Fluid of Chinese Hamster Ovary Cells during Batch Culture and Its Effect on Recombinant Human Antithrombin III Integrity , 1996, Biotechnology progress.
[36] T. Bibila,et al. In Pursuit of the Optimal Fed‐Batch Process for Monoclonal Antibody Production , 1995, Biotechnology progress.
[37] Philip L. Altman,et al. Respiration and Circulation , 1971 .