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Cation exchange (CEX) chromatography is a form of ion exchange (IEX) chromatography in which a positively charged biomolecule binds to a negatively charged resin. POROS cation exchange resins can be applied in both capture and polishing steps to purify antibodies, proteins, enzymes, and other biomolecules. Their rigid particle design supports high dynamic binding capacity, even under challenging pH and conductivity conditions. These resins have been implemented in processes from small-scale development to commercial manufacturing.
Using stable negatively charged ligands, CEX resins assist with efficient purification of proteins and other biomolecules over a wide range of process conditions. Featuring a tightly controlled pore architecture designed for biologics, POROS cation exchange resins offer:
Figure 1. Binding capacity of POROS XS resin with IgG at 5% breakthrough. High binding capacity is obtained under a wide range of process conditions. Column: 0.46 cm (D) x 20 cm (L); buffer: 20 mM MES; load: 5 mg/mL IgG; flow rate: 300 cm/hr.
Figure 2. POROS XS and HS resins present with similar, high-resolution properties. Column: 1 cm (D) x 20 cm (L); buffer A: 20 mM MES, 25 mM NaCl pH 6.2, buffer B: 20 mM MES, 1 M NaCl pH 6.2; elution: gradient 10%–50% buffer B, 7.5 CV; flow rate: 300 cm/hr; protein mix: chymotrypsinogen A, cytochrome C, and lysozyme.
POROS resins offer an easy, flexible solution for cation exchange chromatography in bind/elute or flow-through modes of operation.
Bind/elute application |
Flow-through application |
Polishing of many biomolecules, such as:
|
Polishing by binding impurities under normal bind/elute conditions:
|
Our POROS cation exchange media portfolio includes both strong and weak acid chemistries, each with its specific operating range.
Resin |
Type of CEX resin |
Surface chemistry |
IgG binding capacity (mg/mL) |
pH range |
Pore size (Angstrom) |
POROS XS |
Strong |
Sulfopropyl |
120 |
1–14 |
1,100 |
POROS HS |
Strong |
Sulfopropyl |
70 |
1–14 |
1,020 |
Cation exchange resins can be applied in capture steps where positively charged proteins and other biomolecules bind to negatively charged groups on the resin surface. This approach facilitiates the efficient recovery of molecules, such as therapeutic proteins and enzymes, during the initial purification process.
These resins are commonly used in polishing steps to reduce impurities that remain after earlier purification. This is standard practice in traditional monoclonal antibody purification platforms. By fine-tuning conditions such as pH and conductivity, researchers can separate closely related variants and improve overall product quality.
Use of the products may vary. For specific use statements, please see product literature.