<p>(–) and (–), absorbance of IgGs at 280 nm before and after modification of IgGs with FITC, respectively; the bars correspond to the relative fluorescence of FITC-IgG<sub>mix</sub> fractions (A). Analysis of a relative efficiency of specific-molecule exchange under different conditions between non-modified IgG<sub>mix</sub> and FITC-IgG<sub>mix</sub> having different affinity for DNA-cellulose (B–D). Before chromatography, the IgG<sub>mix</sub> eluted from DNA-cellulose by 0.15 M NaCl (0.15 M-IgG<sub>mix</sub>) were incubated with FITC-IgG<sub>mix</sub> eluted by 1.5 M NaCl (1.5 M-FITC-IgG<sub>mix</sub>) in the presence of TBS and GSH (B); 0.5 M-IgG<sub>mix</sub> and 1.5 M-FITC-IgG<sub>mix</sub> (C) or 0.5 M-FITC-IgG<sub>mix</sub> +1.5 M-...
The selective binding of the cellulose binding domain (CBD) of the exo-ß-l,4-gIycanase Cex from Cel...
<p>The arrows (lane 1) indicate the positions of molecular mass markers. In-gel assay of DNase activ...
none3Recovery of antibodies with Protein A affinity chromatography columns has become the standard f...
<p>(–) and (- - -), absorbance of sIgA<sub>mix</sub> at 280 nm before and after modification of sIgA...
<p>(–) and (–), absorbance of IgGs at 280 nm before and after phosphorylation using γ-[<sup>32</sup>...
<p>Various IgG fractions were separated using DNA-cellulose (A) and ATP-Sepharose (B): (–), absorban...
<p>The analysis was performed after non-labeled pIgG<sub>mix</sub> incubation with preparations of s...
<p>Different IgG fractions were separated using casein-Sepharose (A) and lipid-resin (B): (–), absor...
<p>The chromatography was performed under the conditions of over-saturation of the affinity capacity...
<p>sIgA-1 preparation was chromatographed on DNA-cellulose (A) and ATP-Sepharose (B) in standard con...
<p>Affinity chromatography of milk sIgA-1 preparation on anti-κ-L-Sepharose under the conditions of ...
<p>After chromatography of sIgA-2 and sIgA-3 preparations on DNA-cellulose (A and B, respectively), ...
Affinity columns suitable for HPLC were prepared by immobilization of various ligands of protein A, ...
<p>The analysis was performed using a direct (A) and sandwich (B) ELISA. For a direct analysis, the ...
<p>Hydrophobic chromatography of sIgA<sub>mix</sub> (equimolar mixture of Abs from five donors) on p...
The selective binding of the cellulose binding domain (CBD) of the exo-ß-l,4-gIycanase Cex from Cel...
<p>The arrows (lane 1) indicate the positions of molecular mass markers. In-gel assay of DNase activ...
none3Recovery of antibodies with Protein A affinity chromatography columns has become the standard f...
<p>(–) and (- - -), absorbance of sIgA<sub>mix</sub> at 280 nm before and after modification of sIgA...
<p>(–) and (–), absorbance of IgGs at 280 nm before and after phosphorylation using γ-[<sup>32</sup>...
<p>Various IgG fractions were separated using DNA-cellulose (A) and ATP-Sepharose (B): (–), absorban...
<p>The analysis was performed after non-labeled pIgG<sub>mix</sub> incubation with preparations of s...
<p>Different IgG fractions were separated using casein-Sepharose (A) and lipid-resin (B): (–), absor...
<p>The chromatography was performed under the conditions of over-saturation of the affinity capacity...
<p>sIgA-1 preparation was chromatographed on DNA-cellulose (A) and ATP-Sepharose (B) in standard con...
<p>Affinity chromatography of milk sIgA-1 preparation on anti-κ-L-Sepharose under the conditions of ...
<p>After chromatography of sIgA-2 and sIgA-3 preparations on DNA-cellulose (A and B, respectively), ...
Affinity columns suitable for HPLC were prepared by immobilization of various ligands of protein A, ...
<p>The analysis was performed using a direct (A) and sandwich (B) ELISA. For a direct analysis, the ...
<p>Hydrophobic chromatography of sIgA<sub>mix</sub> (equimolar mixture of Abs from five donors) on p...
The selective binding of the cellulose binding domain (CBD) of the exo-ß-l,4-gIycanase Cex from Cel...
<p>The arrows (lane 1) indicate the positions of molecular mass markers. In-gel assay of DNase activ...
none3Recovery of antibodies with Protein A affinity chromatography columns has become the standard f...