Polysulphone (PS) was chemically modified by acrylation-amination and by chloromethylation-amination, respectively. An ultrafiltration membrane of chemically modified polysulphone (CMPS) was prepared by the phase inversion method. Trypsin was then covalently bonded onto the CMPS membrane by diazotization. The activity of immobilized trypsin reaches up to 10200 U/g; 15 mg trypsin was immobilized on 1 g CMPS membrane. Separation of soybean trypsin inhibitor was carried out on the affinity membrane, yielding 6.5 mg pure trypsin inhibitor in one run. The enzyme membrane has good activity and stability
Abstract This work established the conditions of covalent immobilization of trypsin on a Sepharose ...
Downstream purification processes for monoclonal antibody production typically involve multiple step...
One-step purification of biomolecules from complex feed is challenging with commercial membrane adso...
Affinity columns suitable for HPLC were prepared by immobilization of various ligands of protein A, ...
This study aimed to investigate the significance of the physico-chemical environment during trypsin ...
Endotoxin was removed by membrane affinity chromatography. Macropore cellulose membrane was prepared...
This study aimed to investigate the significance of the physico-chemical environment during trypsin ...
Chromatographic separation of protein mixtures has become one of the most effective widely used mean...
WOS: 000221573700019PubMed: 15135107Two different dye-ligands, i.e. Procion Brown MX-5BR (RB-10) and...
WOS: 000223925200002A poly(hydroxyethylmethacrylate)/chitosan (pHEMA-chitosan) composite membrane wa...
High-performance affinity matrices were obtained by attaching pseudobiospecific ligands to hollow-fi...
A new iminodiacetic acid (IDA) type chelating membrane based on composite matrix formed by covalentl...
Three active forms of autolyzed porcine trypsin, delta-, gamma- and sigma-trypsins, have been isolat...
In order to study the mechanism of substrate binding of trypsin by affinity chromatography, we synth...
A novel chromatographic support denoted as an immobilized artificial membrane (IAM) has been designe...
Abstract This work established the conditions of covalent immobilization of trypsin on a Sepharose ...
Downstream purification processes for monoclonal antibody production typically involve multiple step...
One-step purification of biomolecules from complex feed is challenging with commercial membrane adso...
Affinity columns suitable for HPLC were prepared by immobilization of various ligands of protein A, ...
This study aimed to investigate the significance of the physico-chemical environment during trypsin ...
Endotoxin was removed by membrane affinity chromatography. Macropore cellulose membrane was prepared...
This study aimed to investigate the significance of the physico-chemical environment during trypsin ...
Chromatographic separation of protein mixtures has become one of the most effective widely used mean...
WOS: 000221573700019PubMed: 15135107Two different dye-ligands, i.e. Procion Brown MX-5BR (RB-10) and...
WOS: 000223925200002A poly(hydroxyethylmethacrylate)/chitosan (pHEMA-chitosan) composite membrane wa...
High-performance affinity matrices were obtained by attaching pseudobiospecific ligands to hollow-fi...
A new iminodiacetic acid (IDA) type chelating membrane based on composite matrix formed by covalentl...
Three active forms of autolyzed porcine trypsin, delta-, gamma- and sigma-trypsins, have been isolat...
In order to study the mechanism of substrate binding of trypsin by affinity chromatography, we synth...
A novel chromatographic support denoted as an immobilized artificial membrane (IAM) has been designe...
Abstract This work established the conditions of covalent immobilization of trypsin on a Sepharose ...
Downstream purification processes for monoclonal antibody production typically involve multiple step...
One-step purification of biomolecules from complex feed is challenging with commercial membrane adso...