GE17-0978-02
Butyl-s Sepharose™ 6 Fast Flow
Cytiva 17-0978-02, pack of 200 mL
About This Item
Recommended Products
ligand
butyl-S
packaging
pack of 200 mL
manufacturer/tradename
Cytiva 17-0978-02
matrix
6% cross-linked agarose
particle size
45-165 μm
average diameter
90 μm
cleaning in place
2-14
working range
3-13
suitability
suitable for bioprocess medium
General description
Application
This resin is designed for the binding and elution of relatively strong hydrophobic molecules at comparatively Low salt concentrations. Butyl?S Sepharose™ 6 Fast FLow is particularly useful during the initial stages of a separation process to remove the bulk of impurities without stringent requirements for conditioning of the sample (e.g. adjustment of pH, salt concentration etc.)
Butyl-S Sepharose™ 6 Fast FLow is available in a range of different bulk pack sizes and convenient pre-packed formats for easy scale-up and process development. As member of the BioProcess media range, Butyl-S Sepharose™ 6 Fast FLow meets industrial demands with security of supply and comprehensive technical and regulatory support.
Features and Benefits
- Binds and elutes relatively strong hydrophobic molecules at comparatively Low salt concentrations
- The least hydrophobic medium in the well proven Sepharose™ Fast FLow HIC range
- Purifies recombinant Hepatitis B virus surface antigen from CHO cells
- Developed and optimized in cooperation with a process-scale manufacturer of biopharmaceuticals
- The hydrophilic nature of the base matrix ensures Low levels of non-specific binding.
Storage and Stability
Analysis Note
Legal Information
Signal Word
Warning
Hazard Statements
Precautionary Statements
Storage Class Code
3 - Flammable liquids
Certificates of Analysis (COA)
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Articles
Optimize salt conditions for protein binding and impurity passage in chromatography to achieve required selectivity.
Optimize salt conditions for protein binding and impurity passage in chromatography to achieve required selectivity.
Optimize salt conditions for protein binding and impurity passage in chromatography to achieve required selectivity.
Optimize salt conditions for protein binding and impurity passage in chromatography to achieve required selectivity.
Protocols
This page discusses various aspects of sample preparation for chromatographic purification.
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