PROCESS DEVELOPMENT AND KINETIC ANALYSIS OF A PROTEIN-FREE HYBRIDOMA PERFUSION SYSTEM

[1]  J. Young,et al.  Effect of Culture Conditions on IgM Antibody Structure, Pharmacokinetics and Activity , 1993, Bio/Technology.

[2]  R. Lemieux,et al.  Hybridoma perfusion systems: A comparison study , 1992, Biotechnology and bioengineering.

[3]  J. Côté,et al.  High-performance gel permeation chromatographic analysis of immunoglobulin M produced by hybridoma cell culture , 1992 .

[4]  R. Lemieux,et al.  Long‐term perfusion culture of hybridoma: A “grow or die” cell cycle system , 1991, Biotechnology and bioengineering.

[5]  M. Doko,et al.  CONSEQUENCES of FOULING and MACROMOLECULE ADSORPTION ONTO ULTRAFILTRATION MEMBRANE FOR PINEAPPLE JUICE PROCESSING , 1991 .

[6]  B. Maiorella,et al.  Crossflow microfiltration of animal cells , 1991, Biotechnology and bioengineering.

[7]  Daniel I. C. Wang,et al.  Effects of paddle impeller geometry on power input and mass transfer in small‐scale animal cell culture vessels , 1989, Biotechnology and bioengineering.

[8]  D. Tidd,et al.  Partial protection of oncogene, anti-sense oligodeoxynucleotides against serum nuclease degradation using terminal methylphosphonate groups. , 1989, British Journal of Cancer.

[9]  R. Lemieux,et al.  Characterization of higher avidity monoclonal antibodies produced by murine B-cell hybridoma variants selected for increased antigen binding of membrane Ig. , 1988, Journal of immunology.

[10]  E. Schlaeger,et al.  Proteolytic activity in the culture supernatants of mouse hybridoma cells. , 1987, Developments in biological standardization.

[11]  M. C. Archer,et al.  The Effect of Temperature on the Flux from a Stirred Ultrafiltration Cell , 1976 .