Transcriptome Analysis of CHO Cell Size Increase During a Fed‐Batch Process

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Transcriptome Analysis of CHO Cell Size Increase During a Fed‐Batch Process ; volume:14 ; number:3 ; year:2019 ; extent:12
Biotechnology journal ; 14, Heft 3 (2019) (gesamt 12)

Creator: Pan, Xiao
Alsayyari, Abdulaziz A.
Dalm, Ciska
Hageman, Jos A.
Wijffels, René H.
Martens, Dirk E.

DOI: 10.1002/biot.201800156

URN: urn:nbn:de:101:1-2022080708370292369190

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

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Pan, Xiao
Alsayyari, Abdulaziz A.
Dalm, Ciska
Hageman, Jos A.
Wijffels, René H.
Martens, Dirk E.

Other Objects (12)

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

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Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

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Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

Hochschulschrift

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

Hochschulschrift

Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

Hochschulschrift

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

Hochschulschrift

Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

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Transcriptome Analysis of CHO Cell Size Increase During a Fed‐Batch Process

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Other Objects (12)

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

Selection of chemically defined media for CHO cell fed-batch culture processes

Metabolic characterization of a CHO cell size increase phase in fed-batch cultures

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

The successful transfer of a modern CHO fed-batch process to different single-use bioreactors

Dissecting cell death pathways in fed‐batch bioreactors

Diffusion-driven fed-batch fermentation in perforated ring flasks

High-cell-density fed-batch cultivations of Vibrio natriegens

Profiling of glycosylation gene expression in CHO fed-batch cultures in response to glycosylation-enhancing medium components

Exploring the limits of conventional small-scale CHO fed-batch for accelerated on demand monoclonal antibody production

Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures

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