GE17-0510-01
Q Sepharose™ Fast Flow
Cytiva 17-0510-01, pack of 300 mL
Synonym(s):
Sepharose fast flow
About This Item
Recommended Products
ligand
quaternary amine
description
Ion Exchanger Type (value)
packaging
pack of 300 mL
manufacturer/tradename
Cytiva 17-0510-01
matrix
6% cross-linked agarose
particle size
45-165 μm
average diameter
90 μm
cleaning in place
2-14
working range
2-12
suitability
suitable for bioprocess medium
General description
Q Sepharose™ Fast Flow is part of the Sepharose™ Fast Flow ion exchange platform, which has been the industrial standard for ion exchange chromatography during recent decades. It is composed of crosslinked 6% agarose beads, with quaternary ammonium (Q) strong anion exchange groups. Q Sepharose™ Fast Flow has high chemical stability, allowing well proven cleaning-in-place (CIP) and sanitization protocols. Scale-up with Q Sepharose™ Fast Flow is straight forward and the medium is available in a range of pre-packed process development tools.
As member of the BioProcess media range, Q Sepharose™ Fast Flow meets industrial demands with security of supply and comprehensive technical and regulatory support.
Features and Benefits
- Well-proven strong anion exchanger developed for industrial downstream processes.
- Used extensively for capture and intermediate purification of a wide range of approved biopharmaceuticals
- The industry standard for ion exchange chromatography during recent decades
- High chemical stability allows for well proven CIP and sanitization protocols
- The hydrophilic nature of the base matrix ensures low levels of non-specific binding leading to low levels of host cell-derived impurities in the elution pool.
Storage and Stability
Analysis Note
Legal Information
Signal Word
Warning
Hazard Statements
Precautionary Statements
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Certificates of Analysis (COA)
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Protocols
This page discusses various aspects of sample preparation for chromatographic purification.
This page covers the use of Sepharose Fast Flow for purification of proteins.
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