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Package | 5/PK/10/PK |
Full name | Ni-NTA 6FF(Pre-Packed Gravity Column),1mL |
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 | 1 mL (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 | 1 mL (5/10 columns) |
2~8°C, do not freeze
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