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Dive into the research topics where Michael J. Comer is active.

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Featured researches published by Michael J. Comer.


Cytotechnology | 1990

Industrial production of monoclonal antibodies and therapeutic proteins by dialysis fermentation

Michael J. Comer; Michael J. Kearns; J. Wahl; Michael John Munster; Thomas Dr. Lorenz; Berthold Szperalski; Stefan Koch; Ulrich Behrendt; Herwig Brunner

A novel and powerful fermentation method is reported for the large-scale growth of mammalian cells and their secreted products. The system described illustrates many of the advantages of conventional batch fermentation processes but in addition has been shown to yield cell densities in excess of 1×107 cells/ml with concomitant increase in product concentration.


Cytotechnology | 1994

Mass spectrometry: a tool for on-line monitoring of animal cell cultures

Ulrich Behrendt; Stefan Koch; Daniel D. Gooch; Ulrich Steegmans; Michael J. Comer

The magnetic sector mass spectrometer is able to detect oxygen uptake and carbon dioxide production rates from animal cell cultivations performed in 101 biorectors. Such data have not been available with the use of classic exhaust gas analysis applying paramagnetic analyzers and infra-red sensors due to the insensitivity of the apparatus available. In the course of the present work we were able to demonstrate, that the oxygen uptake rate correlates to the number of viable cells. Additionally oxygen uptake rates supplied on-line information about the actual physiology of the cells: When the rates changed during the cultivation process, this immediately indicated the occurrence of limitations of components in the medium. The information could be useful in timing key events, such as performing splits or harvesting the bioreactor.


Bioprocess Engineering | 1991

A high density culture system for the in-vitro production of human and mouse monoclonal antibodies

Michael John Munster; Michael J. Kearns; Ulrich Steegmans; Ulrich Behrendt; Michael J. Comer

A simple high density cell culture system is described which demonstrates many of the features of commercially available hollow-fibre systems, but without the need to invest in a dedicated system. The system has been shown to achieve product concentrations of up to 40-fold greater than that obtained in batch culture making gram production of MAbs possible with considerable saving on serum costs.


Archive | 1991

Method for mammalian cell culture

Michael J. Kearns; Michael J. Comer; Ulrich Steegmans; Herbert Jungfer


Archive | 1987

Process for culturing biological material

Michael J. Kearns; Michael J. Comer


Gene | 1988

Ksp632I, a novel class-IIS restriction endonuclease from Kluyvera sp. strain 632 with the asymmetric hexanucleotide recognition sequence: 5'-CTCTTC(N)1-3' 3'-GAGAAG(N)4-5'

Bryan J. Bolton; G.G. Schmitz; Michael Jarsch; Michael J. Comer; Christoph Kessler


FEBS Letters | 1985

Asp 718 from a non-pathogenic species of the genus Achromobacter: a KpnI isoschizomer generating DNA-fragments with 5'-protruding ends

Bryan J. Bolton; Georg Nesch; Michael J. Comer; Werner Wolf; Christoph Kessler


Archive | 1988

Restriction endonuclease cleaving palindromic DNA

Bryan J. Bolton; Michael J. Comer; Christoph Kessler; Georg Nesch


Archive | 1988

Process for inactivating recombinant dna

Friedrich Popp; Michael J. Comer; Gunther Schumacher; Michael John Munster; Bodo Seydler


Archive | 1988

PROCESS FOR INACTIVATION OF RECOMBINANT DNA

Friedrich Popp; Michael J. Comer; Gunther Schumacher; Michael John Munster; Bodo Seydler

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