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Volumn 1216, Issue 6, 2009, Pages 902-909
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Effect of phenyl sepharose ligand density on protein monomer/aggregate purification and separation using hydrophobic interaction chromatography
a
BIOGEN
(United States)
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Author keywords
Adsorption isotherm; Aggregate removal; Hydrophobic interaction chromatography; Ligand density; Phenyl sepharose; Preparative chromatography; Protein purification
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Indexed keywords
HYDROPHOBIC INTERACTION CHROMATOGRAPHY;
LIGAND DENSITY;
PHENYL SEPHAROSE;
PREPARATIVE CHROMATOGRAPHY;
PROTEIN PURIFICATION;
ADSORBENTS;
ADSORPTION;
ADSORPTION ISOTHERMS;
AGGREGATES;
CHROMATOGRAPHIC ANALYSIS;
CHROMATOGRAPHY;
COLUMN CHROMATOGRAPHY;
FLOW INTERACTIONS;
GEL PERMEATION CHROMATOGRAPHY;
HYDROPHOBICITY;
ISOTHERMS;
LIGANDS;
PURIFICATION;
SPECIFICATIONS;
HYDROPHOBIC CHROMATOGRAPHY;
ADSORBENT;
MONOMER;
PHENYL SEPHAROSE;
SEPHAROSE;
UNCLASSIFIED DRUG;
ADSORPTION;
ARTICLE;
CHROMATOGRAPHY;
COLUMN CHROMATOGRAPHY;
DENSITY;
ISOTHERM;
LARGE SCALE PRODUCTION;
PERFORMANCE;
PRIORITY JOURNAL;
PROTEIN PURIFICATION;
SEPARATION TECHNIQUE;
ADSORPTION;
AMMONIUM SULFATE;
CHROMATOGRAPHY, LIQUID;
COMPUTER SIMULATION;
FINITE ELEMENT ANALYSIS;
HYDROPHOBICITY;
LIGANDS;
LINEAR MODELS;
MODELS, CHEMICAL;
PROTEIN MULTIMERIZATION;
PROTEINS;
SEPHAROSE;
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EID: 58149474802
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/j.chroma.2008.12.002 Document Type: Article |
Times cited : (27)
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References (30)
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