Display options
Cite
Pan X, Streefland M, Dalm C, et al. Selection of chemically defined media for CHO cell fed-batch culture processes. Cytotechnology. 2016;69(1):39-56doi: 10.1007/s10616-016-0036-5.
Pan, X., Streefland, M., Dalm, C., Wijffels, R. H., & Martens, D. E. (2017). Selection of chemically defined media for CHO cell fed-batch culture processes. Cytotechnology, 69(1), 39-56. https://doi.org/10.1007/s10616-016-0036-5
Pan, Xiao, et al. "Selection of chemically defined media for CHO cell fed-batch culture processes." Cytotechnology vol. 69,1 (2017): 39-56. doi: https://doi.org/10.1007/s10616-016-0036-5
Pan X, Streefland M, Dalm C, Wijffels RH, Martens DE. Selection of chemically defined media for CHO cell fed-batch culture processes. Cytotechnology. 2017 Feb;69(1):39-56. doi: 10.1007/s10616-016-0036-5. Epub 2016 Nov 29. PMID: 27900626; PMCID: PMC5264622.
Copy Download .nbib Format: NLM
Share it on

Cytotechnology. 2017 Feb;69(1):39-56. doi: 10.1007/s10616-016-0036-5. Epub 2016 Nov 29.

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

Cytotechnology

Xiao Pan, Mathieu Streefland, Ciska Dalm, René H Wijffels, Dirk E Martens

Affiliations

  1. Bioprocess Engineering, Wageningen University, PO Box 16, 6700 AA, Wageningen, The Netherlands. [email protected].
  2. Bioprocess Engineering, Wageningen University, PO Box 16, 6700 AA, Wageningen, The Netherlands.
  3. Synthon Biopharmaceuticals BV, Upstream Process Development, PO Box 7071, 6503 GN, Nijmegen, The Netherlands.
  4. Faculty of Biosciences and Aquaculture, Nord University, 8049, Bodø, Norway.

PMID: 27900626 PMCID: PMC5264622 DOI: 10.1007/s10616-016-0036-5

Abstract

Two CHO cell clones derived from the same parental CHO

Keywords: Antibody production; Cell culture medium; Chinese hamster ovary (CHO) cell; Fed-batch; Metabolite profile; Phase transition

References

  1. Curr Opin Biotechnol. 2013 Dec;24(6):1108-15 - PubMed
  2. Int J Pharm. 2012 Nov 1;437(1-2):303-5 - PubMed
  3. Glycobiology. 2009 Sep;19(9):936-49 - PubMed
  4. Nat Biotechnol. 2004 Nov;22(11):1393-8 - PubMed
  5. Biotechnol Bioeng. 2014 Dec;111(12):2466-76 - PubMed
  6. Biotechnol Bioeng. 2000 May 20;68(4):370-80 - PubMed
  7. Physiol Rev. 2009 Jan;89(1):193-277 - PubMed
  8. J Biosci Bioeng. 2015 Jul;120(1):78-84 - PubMed
  9. Biotechnol Prog. 1994 Jan-Feb;10(1):121-4 - PubMed
  10. Biotechnol Prog. 2013 May-Jun;29(3):745-53 - PubMed
  11. Biotechnol Prog. 2009 Sep-Oct;25(5):1353-63 - PubMed
  12. Metab Eng. 2011 Sep;13(5):598-609 - PubMed
  13. Biotechnol Bioeng. 1995 Jun 20;46(6):525-35 - PubMed
  14. J Biotechnol. 2010 Dec;150(4):497-508 - PubMed
  15. N Biotechnol. 2013 Jun 25;30(5):563-72 - PubMed
  16. Biotechnol Bioeng. 2012 May;109(5):1173-86 - PubMed
  17. Biotechnol Bioeng. 2011 May;108(5):1078-88 - PubMed
  18. Metab Eng. 2012 Mar;14(2):138-49 - PubMed
  19. Appl Microbiol Biotechnol. 2003 Dec;63(2):164-73 - PubMed
  20. Biotechnol Prog. 1997 Sep-Oct;13(5):688-91 - PubMed
  21. Biotechnol Bioeng. 2014 May;111(5):965-79 - PubMed
  22. Cytotechnology. 2000 Oct;34(1-2):59-70 - PubMed
  23. J Biotechnol. 2005 May 25;117(3):277-86 - PubMed
  24. Appl Microbiol Biotechnol. 2015 Jun;99(11):4645-57 - PubMed
  25. Biotechnol Bioeng. 2004 Mar 30;85(7):741-9 - PubMed
  26. Biotechnol Bioeng. 2013 Feb;110(2):660-6 - PubMed
  27. Biotechnol Bioeng. 1993 Jan 20;41(2):188-93 - PubMed
  28. Biotechnol Bioeng. 2012 Jan;109(1):146-56 - PubMed

Publication Types