Quantification of immunoglobulin G and characterization of process related impurities using coupled Protein A and size exclusion high performance liquid chromatography

Journal of Chromatography A

Volumn 1217, Issue 31, 2010, Pages 5092-5102

  Horak, Jeannie ^a   Ronacher, Alexander ^a   Lindner, Wolfgang ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

Antibody purification; Bradford; Cell culture supernatant; DNA; Dynamic binding capacity; Protein A; Protein quantification; Size exclusion; Static binding capacity

Indexed keywords

ANTIBODY PURIFICATION; BINDING CAPACITIES; DNA DYNAMICS; PROTEIN A; PROTEIN QUANTIFICATION; SIZE EXCLUSION;

ANTIBODIES; BODY FLUIDS; DNA; GENES; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROJECTILES; PURIFICATION; SIZE EXCLUSION CHROMATOGRAPHY;

CELL CULTURE;

BOVINE SERUM ALBUMIN; IMMUNOGLOBULIN G; PHOSPHATE BUFFERED SALINE; PROTEIN A;

ARTICLE; CELL CULTURE; CONTROLLED STUDY; CULTURE MEDIUM; GEL PERMEATION CHROMATOGRAPHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INTERMETHOD COMPARISON; PHOTOMETRY; PRIORITY JOURNAL; PROTEIN BINDING; PURIFICATION; QUANTITATIVE ANALYSIS; ULTRAVIOLET RADIATION;

ANIMALS; CATTLE; CHROMATOGRAPHY, GEL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; IMMUNOGLOBULIN G; PROTEIN BINDING; SERUM ALBUMIN, BOVINE; STAPHYLOCOCCAL PROTEIN A;

BOVINAE;

EID: 77954564525     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2010.06.007     Document Type: Article

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