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GPB-60(High Density) Butyl Hydrophobic Media (High Density), Highly Cross-Linked Polyacrylate Microspheres, Bogen (CAT#: STEM-C-3053-LGZ)

Highlights

The medium retains the high mechanical strength of the polymer microspheres while having good compatibility with bioactive macromolecules.

Cat Number: STEM-C-3053-LGZ

Application: It is especially suitable for the separation and purification of proteins, enzymes, polysaccharides, nucleic acids, plasmids, etc.

Model: GPB-60(High Density)

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Description

Hydrophobic chromatography utilizes the adsorption of proteins on the hydrophobic groups of the chromatography medium at high salt concentration. When the salt concentration is reduced, different proteins are eluted in order from weak to strong hydrophobicity, so as to achieve the purpose of separation and purification. With mild operating conditions and high resolution, hydrophobic chromatography is one of the most commonly used methods for the separation and purification of biological macromolecules. The GP series of hydrophobic chromatography media developed by Bogen are based on polyacrylate microspheres with high cross-linking degree and Butyl, Octyl, Phenyl, etc. as ligands (the hydrophobicity increases in turn). Isolation and purification of plasmids, etc.

Specification

Matrix: highly cross-linked polyacrylate microspheres
Average particle size: 60μm (50-90μm)
Average pore size: 500nm
Functional groups and ligand density
Butyl: 30 μmol/ml wet gel
Octyl: 5 μmol/ml wet gel
Phenyl: 25 μmol/ml wet gel
Maximum flow rate (25°C): 1000 cm/h
Maximum pressure: 1 MPa (10 bar)
pH stability: 2~13 (long time); 1~14 (short time)
Chemical stability: 1M NaOH, 0.01M HCl, 6M guanidine hydrochloride, 8M urea soaked for 7 days at room temperature, no obvious change in performance
Physical stability: The pH or ionic strength of the solution affects the volume change rate of the medium <0.1%
Storage: 4~30 °C (20% ethanol)

Features

The medium retains the high mechanical strength of the polymer microspheres while having good compatibility with bioactive macromolecules.

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