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Catalog No. CYT28929127
Part No. 28929127
Supplier Cytiva
ReadyToProcess™ Capto™ DEAE 10 L (251/200)
Net Price
Special offer
Availability

4 weeks

PROPERTIES
  • Chromatography technique
    Ion exchange chromatography
  • Bed volume
    10 L
  • Pressure max. (over the packed bed during operation)
    3 bar (0.3 MPa, 44 psi)
  • Pack size
    10 L
  • Bed height
    200 mm
  • Column i.d.
    251
  • Application
    For manufacturing of biopharmaceuticals for clinical phase I and II studies. Depending on the scale of operations, they can also be used for full-scale manufacturing, as well as for preclinical studies.
  • Storage
    4°C to 30°C, 20% ethanol
  • Bed dimensions
    251 × 200 mm
  • Certificate of Analysis
    Yes
DESCRIPTION
Our Capto™ DEAE weak anion exchange chromatography resin for large-scale manufacturing is prepacked in ReadyToProcess™ columns for fast, cost-effective capture and intermediate protein purification. Validated, high-performance bioprocess columns supplied prepacked and ready for use in ion exchange chromatography applications. High throughput for optimized productivity and process economy. Flexible process design with large operational window of flow velocities and bed heights. Excellent chemical stability. Meets industrial demands for security of supply, robust performance, and regulatory support. Capto™ DEAE resins Capto™ DEAE weak anion exchange chromatography resin is designed for fast, cost-effective capture and intermediate protein purification in large-scale manufacturing. Weak anion exchange resin for high-productivity capture and intermediate purification when high-volume throughput is essential. High dynamic binding capacity at high flow raises productivity. High-volume throughput cuts process times. Cost-effective processing with smaller unit operations. ReadyToProcess™ chromatography columns Packed with validated methods for consistent performance. Standardized format keeps costs low delivery lead times short. Ready to use without the need for column packing, preparation, and validation procedures.
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