Description
Amine-PEG-NTA a heterobifunctional polyethylene glycol (PEG) linker featuring a primary amine group at one terminus and a nitrilotriacetic acid (NTA) group at the other. It is designed for the oriented immobilization or labeling of recombinant proteins containing a polyhistidine (His-tag) sequence. The primary amine enables covalent conjugation to carboxyl groups on surfaces, nanoparticles, or biomolecules via carbodiimide chemistry (e.g., EDC/NHS), while the NTA moiety, when charged with divalent metal ions (typically Ni²⁺ or Co²⁺), provides high-affinity, reversible binding to His-tagged proteins through metal coordination. The PEG spacer enhances water solubility, reduces non-specific binding, and offers steric flexibility. This reagent is widely used in biosensor development, protein microarray fabrication, nanoparticle functionalization, and the construction of oriented protein conjugates where controlled orientation via the His-tag is required.
Properties
Custom synthesis is available for PEG-NTA including:
mPEG-NTA MW 350, 550, 750, 1k, 2k, 5k, 10k, 20k, 30k and 40k
NTA-PEG-NTA MW 600, 1k, 2k, 3.4k, 5k, 10k, 20k and 30k
4-arm PEG-NTA MW 2k, 5k, 10k and 20k
8-arm PEG-NTA MW 10k, 20k and 40k
Maleimide-PEG-NTA MW 1k, 2k, 3.4k, 5k and 10k
Acrylate-PEG-NTA MW 1k, 2k, 3.4k, 5k and 10k
Biotin-PEG-NTA MW 1k, 2k, 3.4k, 5k and 10k
FITC-PEG-NTA MW 1k, 2k, 3.4k, 5k and 10k
and many others
References
His-tag and Ni-NTA (Nickel-Nitrilotriacetic acid) are fundamental components for recombinant protein purification, relying on the strong, specific binding between a short string of histidine residues (the His-tag) and immobilized nickel ions on a resin (Ni-NTA). This technique, called Immobilized Metal Affinity Chromatography (IMAC), uses Ni-NTA’s high affinity for the tag to capture target proteins from complex cell lysates, allowing easy purification under native or denaturing conditions for downstream applications like detection or functional studies.