| Chromatography technique | Ion Exchange Chromatography |
|---|---|
| Avoid Using | Oxidizing agents, cationic detergents |
| Binding Capacity/ml Chromatography Medium | > 70 mg lysozyme, > 95 mg BSA |
| BioProcess resin | Yes |
| Certificate of Analysis | Yes |
| Chemical stability | Commonly used aqueous buffers, 1 M NaOH, 8 M urea, 6 M guanidine hydrochloride, 30% isopropanol and 70 % ethanol |
| Ion Exchanger Type | Strong cation exchanger |
| Ionic Capacity | 0.13-0.16 mmol H + /ml medium |
| Ligand | Sulfopropyl group |
| Matrix | High-flow agarose |
| Particle Size | 36-44 μm (d 50V ) |
| Pressure/Flow Specification | 300 kPa at min. 220 cm/h, 1 m diameter column, 20 cm bed height |
| Storage | 4 to 30°C, 20% Ethanol + 0.2 M Sodium Acetate |
| pH stability, CIP | 3–14 |
| pH stability, operational | 4–12 |
Answer:No. It is a strong cation exchanger with sulfopropyl functional groups.
Answer:The high-resolution agarose beads have an approximate average particle size of 40 µm.
Answer:It is used mainly for intermediate purification and polishing where close charge-based separation matters.
Capto SP ImpRes is a strong cation exchange chromatography resin designed for high-resolution protein purification at intermediate and polishing stages. This 100 mL presentation supports laboratory-scale preparative work, evaluation of product-related variants and method transfer after initial screening. Its sulfopropyl ligand is immobilized on a high-flow agarose matrix with particles approximately 40 µm in diameter. The smaller bead size supports sharper separation of closely related charged species than a coarser capture-oriented resin, while column packing and operating pressure still influence performance. Antibodies and other proteins can be resolved by controlling sample conductivity, binding pH and salt-gradient shape. The resin is particularly useful when the objective is to reduce charge variants, process impurities or aggregates with different retention characteristics. Optimize loading and elution using measured chromatograms rather than assuming all proteins share the same binding profile. Supplied as bulk resin for packing, not as a membrane adsorber.
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