Nitrilotriacetic acid (NTA)-crosslinked-agarose resin consists of NTA groups covalently immobilized on agarose beads by stable ether linkages via a spacer arm. NTA is a tetradentate chelating agent forms an octahedral coordination complex with divalent transition metal cations (Co2+) along with two water molecules occupied in cis manner. This ready to use resin, after loading with a divalent transition metal ion (Co2+) is ideal for rapid purifications of His-tagged proteins. In comparison with other chelating resins such as iminodiacetic acid (IDA)-agarose, the NTA has two sites (cis) available for the interaction with imidazole of His-tagged proteins, instead of the three in IDA, and so have a lesser probability of nonspecific binding. NTA resins are usually more easily regenerated, allowing a better elution of the fused proteins bound with smaller concentrations of imidazole.
Though Ni-resin is being widely used for His-tag recombinant protein purification but in some cases, Co-resins is preferable due to its higher specificity. Where purity is of prior importance over quantity, it is recommended to use Co-resins for better results. The product is supplied as 50% suspension of Co-NTA Agarose resin in 20% aqueous ethanol; the settled bead volume is measured in ml, when supplied.
Co-NTA resins can withstand autoclaving at 120°C for 20 min without any significant loss of binding efficiency.
TECHNICAL SPECIFICATIONS
BEAD GEOMETRY & SIZE: Spherical, Standard
∼ 50-150 μm diameters
CROSS-LINKED: Yes
AGAROSE %: 4%
ACTIVATING GROUP: Epoxy
MATRIX STABILITY: Stable in all commonly used reagents
STORAGE SOLUTION: 20 % Ethanol
STORAGE TEMPERATURE: 4°C to 8°C. DO NOT FREEZE.
For Research use only – Not for use in diagnostics procedures.







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