Literature DB >> 8765172

The protein hydrolysate, Primatone RL, is a cost-effective multiple growth promoter of mammalian cell culture in serum-containing and serum-free media and displays anti-apoptosis properties.

E J Schlaeger1.   

Abstract

The tryptic meat digest Primatone RL is a low-cost medium supplement of a complex nature which serves as a source of amino acids, oligopeptides, iron salts, some lipids and other trace low molecular weight substances. Its addition to mammalian and insect cell culture media significantly improves the cell growth properties of many cell lines. In this work the growth promoting effects of Primatone RL are described in more detail using different mouse hybridomas, a mouse myeloma cell line, and human promyelocytic leukemia HL-60 cells. The positive effects on cell growth induced by Primatone were observed in the presence of serum but were even more pronounced in serum-free culture. In addition the adaptation time from high serum to low (1%) or serum-free growth in the presence of Primatone is also significantly reduced. Primatone RL, when added to HL and DHI medium, improves cell growth under low serum or serum-free conditions by increasing the maximum cell numbers and in particular the viability of the culture. The observed decrease in cell death (apoptosis) induction leads to a significant improvement in antibody (recombinant protein) production by increasing the volumetric yields during long-term batch culture. The so-called anti-apoptotic effects of Primatone RL for mouse hybridomas, which is concentration dependent, is not fully understood.

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Year:  1996        PMID: 8765172     DOI: 10.1016/0022-1759(96)00080-4

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  24 in total

1.  Overexpressing human membrane proteins in stably transfected and clonal human embryonic kidney 293S cells.

Authors:  Sarika Chaudhary; John E Pak; Franz Gruswitz; Vinay Sharma; Robert M Stroud
Journal:  Nat Protoc       Date:  2012-02-09       Impact factor: 13.491

2.  Medium design for insect cell culture.

Authors:  E J Schlaeger
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

3.  On-line monitoring of responses to nutrient feed additions by multi-frequency permittivity measurements in fed-batch cultivations of CHO cells.

Authors:  Sven Ansorge; Geoffrey Esteban; Georg Schmid
Journal:  Cytotechnology       Date:  2010-04-21       Impact factor: 2.058

4.  Effect of Partial Medium Replacement on Cell Growth and Protein Production for the High-Fivetrade mark insect cell line.

Authors:  Laertis Ikonomou; Georges Bastin; Yves-Jacques Schneider; Spiros N Agathos
Journal:  Cytotechnology       Date:  2004-01       Impact factor: 2.058

5.  Development of a generic transient transfection process at 100 L scale.

Authors:  Ola Tuvesson; Christina Uhe; Aleksei Rozkov; Elke Lüllau
Journal:  Cytotechnology       Date:  2008-02-22       Impact factor: 2.058

6.  Promoting effect of rapeseed proteins and peptides on Sf9 insect cell growth.

Authors:  V Deparis; C Durrieu; M Schweizer; I Marc; J L Goergen; I Chevalot; A Marc
Journal:  Cytotechnology       Date:  2003-07       Impact factor: 2.058

7.  The new medium MDSS2N, free of any animal protein supports cell growth and production of various viruses.

Authors:  O W Merten; H Kallel; J C Manuguerra; M Tardy-Panit; R Crainic; F Delpeyroux; S Van der Werf; P Perrin
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

8.  The use of peptones as medium additives for the production of a recombinant therapeutic protein in high density perfusion cultures of mammalian cells.

Authors:  R Heidemann; C Zhang; H Qi; J Larrick Rule; C Rozales; S Park; S Chuppa; M Ray; J Michaels; K Konstantinov; D Naveh
Journal:  Cytotechnology       Date:  2000-02       Impact factor: 2.058

9.  A T-flask based screening platform for evaluating and identifying plant hydrolysates for a fed-batch cell culture process.

Authors:  Canghai Lu; Carlos Gonzalez; Joseph Gleason; Jennifer Gangi; Jeng-Dar Yang
Journal:  Cytotechnology       Date:  2007-08-18       Impact factor: 2.058

10.  Combination of yeast hydrolysates to improve CHO cell growth and IgG production.

Authors:  Mathilde Mosser; Isabelle Chevalot; Eric Olmos; Fabrice Blanchard; Romain Kapel; Eric Oriol; Ivan Marc; Annie Marc
Journal:  Cytotechnology       Date:  2012-12-14       Impact factor: 2.058

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