GE17-1287-01
Anx Seph 4 Fast Flow High Sub
Cytiva 17-1287-01, pack of 500 mL
About This Item
Recommended Products
ligand
diethylaminopropyl
description
Ion Exchanger Type (value)
packaging
pack of 500 mL
manufacturer/tradename
Cytiva 17-1287-01
matrix
4% 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
Related Categories
General description
Application
As member of the BioProcess media range, ANX Sepharose™ 4 Fast FLow (high sub) meets industrial demands with security of supply and comprehensive technical and regulatory support.
Features and Benefits
- Weak anion exchanger with different selectivity compared with traditional ion exchangers.
- Applicable for separation of high molecular weight Proteins
- Developed in co-operation with leading large-scale pharmaceutical manufacturers
- 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
Certificates of Analysis (COA)
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Articles
This page shows volatile and non-volatile buffer suggestions for anion and cation exchange chromatography.
This page covers the standard ÄKTAdesign configurations for simple IEX chromatography.
This page covers practical problems that may lead to a non-ideal IEX separation and their solutions.
This page covers detailed aspects of each step in an IEX separation to improve resolution and overall performance.
Protocols
This page covers the use of Sepharose Fast Flow for purification of proteins.
This page shows how to perform column packing and preparation for ion exchange chromatography and chromatafocusing when using Tricorn or XK columns available from Cytiva.
This page clarifies sample preparation, buffer exchange and desalting, removal of lipoproteins, phenol red, and low molecular weight contaminants in Ion exchange chromatography.
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