Investigating the influence of physiologically relevant hydrostatic pressure on CHO cell batch culture
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Investigating the influence of physiologically relevant hydrostatic pressure on CHO cell batch culture ; volume:11 ; number:1 ; day:8 ; month:1 ; year:2021 ; pages:1-9 ; date:12.2021
Scientific reports ; 11, Heft 1 (8.1.2021), 1-9, 12.2021
- Urheber
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-020-80576-8
- URN
-
urn:nbn:de:101:1-2021020523410097896595
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:36 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Shang, Menglin
- Kwon, Taehong
- Hamel, Jean-Francois P.
- Lim, Chwee Teck
- Khoo, Bee Luan
- Han, Jongyoon
- SpringerLink (Online service)
Ähnliche Objekte (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
Cho-Cho San
Cho-Cho San
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
bAtch BATCH
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
Caspase activation, sialidase release and changes in sialylation pattern of recombinant human erythropoietin produced by CHO cells in 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
Cho-Cho San
Cho-Cho San
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
bAtch BATCH
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
Caspase activation, sialidase release and changes in sialylation pattern of recombinant human erythropoietin produced by CHO cells in 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
Cho-Cho San
Cho-Cho San
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
Use of S-sulfocysteine (SSC) as a L-cysteine source in Chinese hamster ovary (CHO) suspension batch and fed-batch cultures
bAtch BATCH
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