๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Development of a hollow-fiber system for large-scale culture of mammalian cells

โœ Scribed by K. Ku; M. J. Kuo; J. Delente; B. S. Wildi; J. Feder


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
750 KB
Volume
23
Category
Article
ISSN
0006-3592

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

A flatโ€bed hollowโ€fiber cell culture system has been developed which maximizes the utilization of the large fiber surface while diminishing significantly the problems inherent in a cartridgeโ€type reactor. The reactor core consists of a shallow bed of hollow fibers sandwiched between two stainlessโ€steel microporous filter plates through which the media flow is directed normal to the plane of the fiber bed. Reactors with both 930 and 9300 cm^2^ of fiber surface have been successfully constructed and operated. A variety of cells has been grown in these reactors including SV3T3 cells, baby hamster kidney cells, Vero cells, and rhesus money kidney cells, and cell products such as plasminogen activator and migration inhibition factor (MIF) were produced. This system offers an excellent prototype for scaleup design.


๐Ÿ“œ SIMILAR VOLUMES


Development of optimized transfectoma ce
โœ Beatrice S. Schlรคpfer; Marcel Scheibler; Anke-Peggy Holtorf; Hai Van Nguyen; Ger ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 987 KB

Methods for the selection of transfectoma cells that express large quantities of mouse-human chimeric antibodies have been developed. SP2/0 mouse myeloma cells were transfected with pSV2-gpt and pSV2-neo based immunoglobulin expression vectors. Double transfectants were selected using the xanthinegu

Large-scale production of endotoxin-free
โœ Aleksei Rozkov; Bert Larsson; Stefan Gillstrรถm; Robert Bjรถrnestedt; Stefan R. Sc ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 219 KB ๐Ÿ‘ 2 views

## Abstract Transient expression of recombinant proteins in mammalian cell culture in a 100โ€L scale requires a large quantity of plasmid that is very labour intensive to achieve with shake flask cultures and commercially available plasmid purification kits. In this paper we describe a process for p