Trigoats Tech’s affinity chromatography media were prepared by monodisperse, highly crosslinked polyacrylate microspheres. The affinity chromatography media are produced by first forming a hydrophilic layer on the microspheres. Then, nickel ion (Ni2+) functional groups are chelated onto the hydrophilic layer. Trigoats Tech’s affinity chromatography media have high selectivity in separation of histidine labeled proteins.
Table 1: List of affinity chromatography media
Product Name | Particle Size(μm)(μm) | Type ligands | Functional Groups | Pore Size(Å) |
QY-30Ni-IDA | 30 | IDA | Ni2+ | 800 |
QY-50Ni-IDA | 50 | IDA | Ni2+ | 800 |
QY-30Ni-NTA | 30 | NTA | Ni2+ | 800 |
QY-50Ni-NTA | 50 | NTA | Ni2+ | 800 |
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