Characterization of the stability of recombinant protein production in the GS-NS0 expression system.
about
Intraclonal protein expression heterogeneity in recombinant CHO cellsProduction of recombinant protein therapeutics in cultivated mammalian cells.Development of an improved mammalian overexpression method for human CD62LThe selection of high-producing cell lines using flow cytometry and cell sorting.Evaluating the use of a CpG free promoter for long-term recombinant protein expression stability in Chinese hamster ovary cells.Using cell engineering and omic tools for the improvement of cell culture processes.An 'omics approach towards CHO cell engineering.Ubiquitous Chromatin Opening Elements (UCOEs) effect on transgene position and expression stability in CHO cells following methotrexate (MTX) amplification.A BioDesign Approach to Obtain High Yields of Biosimilars by Anti-apoptotic Cell Engineering: a Case Study to Increase the Production Yield of Anti-TNF Alpha Producing Recombinant CHO Cells.Improved CHO Cell Line Stability and Recombinant Protein Expression During Long-Term Culture.High levels of histone H3 acetylation at the CMV promoter are predictive of stable expression in Chinese hamster ovary cells.Slashing the timelines: Opting to generate high-titer clonal lines faster via viability-based single cell sorting.Assessment of UCOE on Recombinant EPO Production and Expression Stability in Amplified Chinese Hamster Ovary Cells.Evaluating the interaction between UCOE and DHFR-linked amplification and stability of recombinant protein expression.Early prediction of instability of Chinese hamster ovary cell lines expressing recombinant antibodies and antibody-fusion proteins.A mechanistic understanding of production instability in CHO cell lines expressing recombinant monoclonal antibodies.CMV promoter mutants with a reduced propensity to productivity loss in CHO cells.Bioprocess applications of a Sindbis virus-based temperature-inducible expression system.Production of anti TNF-α antibodies in eukaryotic cells using different combinations of vectors carrying heavy and light chains.Impact of using different promoters and matrix attachment regions on recombinant protein expression level and stability in stably transfected CHO cells.Insertion of core CpG island element into human CMV promoter for enhancing recombinant protein expression stability in CHO cells.Generation of stable, high-producing CHO cell lines by lentiviral vector-mediated gene transfer in serum-free suspension culture.Establishment and characterization of cell clones from the Papilio cell line RIRI-PaDe-3 by a high-efficiency clonal method.
P2860
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P2860
Characterization of the stability of recombinant protein production in the GS-NS0 expression system.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Characterization of the stabil ...... the GS-NS0 expression system.
@en
Characterization of the stabil ...... the GS-NS0 expression system.
@nl
type
label
Characterization of the stabil ...... the GS-NS0 expression system.
@en
Characterization of the stabil ...... the GS-NS0 expression system.
@nl
prefLabel
Characterization of the stabil ...... the GS-NS0 expression system.
@en
Characterization of the stabil ...... the GS-NS0 expression system.
@nl
P2093
P2860
P356
P1476
Characterization of the stabil ...... the GS-NS0 expression system.
@en
P2093
P2860
P304
P356
10.1002/BIT.1059
P577
2001-05-01T00:00:00Z