A novel strategy for quantitative isoform detection directly performed from culture supernatant

Journal of Pharmaceutical and Biomedical Analysis

Volumn 42, Issue 3, 2006, Pages 322-327

  Schriebl, Kornelia ^a   Trummer, Evelyn ^a,b   Weik, Robert ^c   Müller, Dethardt ^b   Kunert, Renate ^b   Lattenmayer, Christine ^a,b   Katinger, Hermann ^b,c   Vorauer Uhl, Karola ^b  

^a Austrian Center of Biopharmaceutical Technology   (Austria)

^b UNIVERSITY OF AGRICULTURAL SCIENCES   (Austria)

^c POLYMUN SCIENTIFIC IMMUNBIOLOGISCHE FORSCHUNG GMBH   (Austria)

Author keywords

CHO cells; CyDye fluors; Fusion protein Epo Fc; Isoelectric focusing; Isoform pattern

Indexed keywords

DYE; GLYCOSYLATED PROTEIN; HUMAN IMMUNOGLOBULIN; HYBRID PROTEIN; IMMUNOGLOBULIN G1; RECOMBINANT ERYTHROPOIETIN;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; CULTURE MEDIUM; ELECTROPHORESIS; FEMALE; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; QUANTITATIVE ASSAY; SAMPLE; SUPERNATANT;

ANIMALS; CHO CELLS; CRICETINAE; ERYTHROPOIETIN, RECOMBINANT; IMMUNOGLOBULIN FC FRAGMENTS; ISOELECTRIC FOCUSING; PROTEIN ISOFORMS; RECOMBINANT FUSION PROTEINS; REPRODUCIBILITY OF RESULTS;

EID: 33747119498     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2006.04.021     Document Type: Article

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