GE17-0729-10
SP Sepharose™ Fast Flow
Cytiva 17-0729-10, pack of 25 mL
Sinónimos:
SP Sepharose Column, Sepharose Fast Flow
About This Item
Productos recomendados
ligand
sulphopropyl
description
Ion Exchanger Type (value)
packaging
pack of 25 mL
manufacturer/tradename
Cytiva 17-0729-10
matrix
6% cross-linked agarose
particle size
45-165 μm
average diameter
90 μm
cleaning in place
3-14
working range
4-13
capacity
70 mg binding capacity(ribonuclease A/ml medium)
suitability
suitable for bioprocess medium
General description
Application
As member of the BioProcess media range, SP Sepharose™ Fast FLow meets industrial demands with security of supply and comprehensive technical and regulatory support.
Features and Benefits
- Well-proven strong cation 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
signalword
Warning
hcodes
Storage Class
3 - Flammable liquids
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Artículos
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This page describes principles and standard conditions for different purification techniques of histidine-tagged proteins using GE Healthcare products.
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.
Protocolos
This page covers the use of Sepharose Fast Flow for purification of proteins.
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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