50 µm 1500 Å Strong Anion-Exchange PS-DVB Medium ~120 mg/mL BSA DBC
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50 µm 1500 Å Strong Anion-Exchange PS-DVB Medium ~120 mg/mL BSA DBC

Cat.No: IGM-HMM-0255 Datasheet

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Product Name 50 µm 1500 Å Strong Anion-Exchange PS-DVB Medium ~120 mg/mL BSA DBC
Catalog No. IGM-HMM-0255
Description The Alta DiagnoTech strong anion-exchange medium uses monodisperse PS-DVB beads with an open macroporous structure. Hydrophilic surface modification reduces nonspecific adsorption, while a quaternary-ammonium ligand provides high-capacity charge-based separation with high mechanical strength.
Intended Use Large-scale purification of monoclonal antibodies, viruses, vaccines and high-molecular-weight recombinant proteins.
Principle / Technology Strong anion-exchange chromatography using a quaternary-ammonium ligand on macroporous PS-DVB beads.
Performance Range / Specifications 50 µm particles; 1,500 Å pores; ligand density approximately 0.25 meq/mL; dynamic binding capacity approximately 120 mg/mL for BSA; maximum pressure 2.0 MPa.
Package Specifications 30 mL, 50 mL, 100 mL, 300 mL, 500 mL, 1 L, 5 L, 10 L, 50 L and 100 L
Product Form PS-DVB strong anion-exchange chromatography medium
Key Features Approximately 120 mg/mL BSA dynamic binding capacity
1,500 Å open macropores
2.0 MPa maximum pressure
pH 1-14 stability
Product Type Strong anion-exchange chromatography medium
Function / Efficacy High-capacity charge-based purification of negatively charged biomolecules.
Customization Prepacked columns are available in 7.7 × 22 mm, 16 × 25 mm and 7.7 × 100 mm formats; additional formats may be customized.
Functional Group Quaternary ammonium
Chromatography Mode Strong anion-exchange chromatography
Matrix Polystyrene-divinylbenzene (PS-DVB)
Particle Size 50 µm
Pore Size 1,500 Å
Ligand / Bonded Phase −CH₂N⁺(CH₃)₃
Dynamic Binding Capacity Approximately 120 mg/mL for BSA
Ligand Density Approximately 0.25 meq/mL
Maximum Operating Pressure 2.0 MPa
CIP / Sanitization Conditions 1 M NaOH
Recommended Flow Rate 50-300 cm/h
pH Stability pH 1-14
Chemical Stability Common buffers, 1 M acetic acid, 1 M NaOH, 1 M HCl, 70% ethanol, 30% isopropanol, 30% acetonitrile, 1% SDS, 6 M guanidine hydrochloride and 8 M urea. Avoid strong oxidants, oxidizing acids, strong reducing agents, acetone and benzyl alcohol.
Operating Temperature 4-30 °C

For research use only, not for clinical use.

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