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Sku: P310132-1/PK
Categories: Hot-sale Products

Specification

Package 1/PK/5/PK/10/PK
Full name Ni-NTA 6FF(Pre-Packed Gravity Column),5mL
Applications Purification of His 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 is chemically fixed to the hydroxyl groups on the surface of agarose using iminodiacetic acid (IDA) molecules, which are then complexed with metal Ni2+by IDA. The purification principle is based on the fact that the imidazole ring labeled with recombinant protein histidine can form stable chemical coordination bonds with transition metal Ni2+ions, thus being able to specifically, firmly, and reversibly adsorb onto the agarose matrix fixed with these metal ions.
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 5 mL (1/5/10 columns)
Substrate 6% agarose
Average Particle Size 0
Particle Size 45 μm~165 μm
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 5 mL (1/5/10 columns)

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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