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Sku: P310129-1 KIT
Categories: Hot-sale Products

Specification

Package 1 KIT
Full name Ni-NTA 6FF Sefinose(TM) Resin Kit
Applications Purification of histidine labeled proteins from various expression sources such as Escherichia coli, yeast, insect cells, and mammalian cells.
Summary The matrix of this medium has an average particle size of 90 μm 6% highly cross-linked agarose of m, with metal ion chelating ligands covalently linked, exhibits good stability. The chelating ligand carries divalent Ni2+, which is the medium for purifying most histidine labeled proteins. The ligand density of this medium has been optimized to ensure high protein binding capacity and high selectivity, while the high flow rate characteristics make it suitable for large-scale purification.
Features Compared to Ni IDA agarose made from trivalent metal ion chelating agent iminodiacetic acid, the non-specific adsorption of Ni NTA agarose is significantly reduced, allowing users to obtain higher purity target proteins; 2. Support column refolding of denatured inclusion body proteins, achieving the effect of simultaneous separation and refolding; 3. Can tolerate a certain concentration of reducing reagents( β- Mercaptoethanol can be used up to 20 mM; 4. The agarose matrix remains stable within the pH range of 2-14 and can withstand repeated in situ cleaning (CIP); 5. Minimal leakage of Ni2+during the purification process; 6. It can be reused and regenerated 5-10 times.
Composition 1Kit (1 ml X 10 columns + 500 ml Elution Buffer + 500 ml Binding/Wash Buffer)
Substrate Highly cross-linked 6% agarose
Average Particle Size 90 μm(45-165 μm)
Particle Size 0
Protein Binding Ability Approximately 10-40 mg histidine labeled protein/1 mL resin
Maximum Flow Rate 150 cm/h
Pressurization 0.3 MPa, 3 bar
Storage Buffer 20% ethanol
Component 1Kit (1 ml X 10 columns + 500 ml Elution Buffer + 500 ml Binding/Wash Buffer)

Storage

2~8°C, do not freeze

Documents

https://cdn.shopifycdn.net/s/files/1/0521/5312/2997/files/P310131_P310132_P310129_P310127_EN_P.pdf

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