产品名称
Ni Sepharose™ High Performance, Cytiva 17-5268-01, pack of 25 mL
crosslinking
cross-linked
packaging
pack of 25 mL
manufacturer/tradename
Cytiva 17-5268-01
storage condition
(20% ethanol)
parameter
150 cm/hr max. flow rate
technique(s)
liquid chromatography (LC): suitable
matrix
highly cross-linked 6% agarose
matrix active group
Nickel
particle size
~34 μm
cleaning in place
2-14(Ni2+ stripped medium.)
operating pH
3-12(Ni²⁺ stripped medium.)
capacity
≥40 mg binding capacity (histidine-tagged protein / ml medium)
separation technique
affinity
storage temp.
2-30°C
Preparation Note
Legal Information
These products are sold under a license from Sigma-Aldrich under patent number EP 1276716 (Metal chelating compositions) and equivalent patents and patent applications in other countries.
Analysis Note
Features and Benefits
- High-performance purification of histidine-tagged proteins
- Negligible leakage of Ni2+ ions.
- High binding capacity, at least 40 mg/mL medium
- Compatible with a wide range of reducing agents, detergents, denaturants and other additives
- 34 μm bead size for improved resolution
General description
Ni Sepharose™ High Performance consists of highly cross-linked agarose beads to which a chelating group has been coupled. This chelating group is precharged with Ni2+, which will selectively retain proteins with exposed histidine groups.
The high stability and broad compatibility of Ni Sepharose™ High Performance maintains biological activity and increases product yield, at the same time as it greatly expands the range of suitable operating conditions.
signalword
Warning
hcodes
存储类别
3 - Flammable liquids
法规信息
商品
Follow established procedures for recombinant protein expression, growth, induction, and cell lysis optimization.
This page shows how to convert between flow velocity and volumetric flow rate in affinity chromatography of antibodies.
This page shows high-throughput screening using His MultiTrap™ HP and His MultiTrap™ FF 96-well filter plates from Cytiva.
This page covers detailed aspects of each step in an IEX separation to improve resolution and overall performance.
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