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

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1753-6561

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Process development and optimization of fed-batch production processes for therapeutic proteins by CHO cells ; volume:7 ; number:6 ; day:4 ; month:12 ; year:2013 ; pages:1-3 ; date:12.2013
BMC proceedings / Biomed Central ; 7, Heft 6 (4.12.2013), 1-3, 12.2013

Creator: Clincke, Marie-Françoise
Harmsen, Mareike
Malphettes, Laetitia

Contributor: SpringerLink (Online service)

DOI: 10.1186/1753-6561-7-S6-P79

URN: urn:nbn:de:101:1-2019063006241514244129

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

Last update: 14.08.2025, 10:55 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Clincke, Marie-Françoise
Harmsen, Mareike
Malphettes, Laetitia
SpringerLink (Online service)

Other Objects (12)

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

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

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

Hochschulschrift

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

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

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

Hochschulschrift

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

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

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

Hochschulschrift

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

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

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

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

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

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

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

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

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

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

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

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

Optimierung von Fed-Batch Bioprozessen durch Phaseneinteilung

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

Related objects

Reset password