<p>A: Typical fractionation chromatogram of 1 gram IVIG on a 90 mL SNA-agarose column, showing the SNA non-binding (-SNA IVIG) flowthrough fraction (FT) and the SNA binding fractions (+SNA IVIG) eluate 1 (E1) and eluate 2 (E2). B: SDS PAGE and C: Lectin Blot (SNA) analysis of the SNA-purified IVIG fractions. IVIG: source IVIG before fractionation, FT: SNA non-binding flowthrough, E1: SNA binding eluate 1, E2: SNA binding eluate 2, NAase IVIG: Neuraminidase treated (desialylated) IVIG, M: molecular marker, red.: gel run under reducing conditions, non red.: gel run under non-reducing conditions.</p
<p>The binding of sialic acid specific lectin (MAA, <i>Maackia amurensis</i>) to A2HSG in (A) untrea...
Lectins are capable of recognizing specific glycan structures and serve as invaluable tools for the ...
Proteins including glycoproteins and lectins play important roles in many biological processes. Ther...
Scheme of the affinity pull-down assay as in Fig 4. IN: sample before fractionation, UB: unbound fra...
<p>Schematic presentation of purification strategy showing various starting materials for SNA-chroma...
A: Scheme of the affinity pull-down assay. IN: sample before fractionation, UB: unbound fraction (Si...
Affinity chromatography is a method which depends essentially on the interaction between the molecul...
The work described here examines displacement phenomena that play a role in lectin affinity chromato...
<p>Dot blots of the two α-Syn-nAbs standard preparations of one IvIG batch and the affinity chromato...
<p>A. Representative LC-MS chromatograms of a IgG sepharose-binding molecule (m/z 1414.3) are shown ...
Virtually all extracellular proteins in humans are glycoproteins and likewise are many biopharmaceut...
Lectin affinity chromatography (LAC) offers a tool that aids purification of cell surface glycoconju...
<p>Comparison of the four chromatographic methods for immunoglobulin isolation that were evaluated i...
Lectins are sugar-binding proteins that can recognize and bind to carbohydrates conjugated to protei...
Lane M, Molecular Marker (Color Prestained Protein Standard, Broad Range, NEB); lane 1, culture supe...
<p>The binding of sialic acid specific lectin (MAA, <i>Maackia amurensis</i>) to A2HSG in (A) untrea...
Lectins are capable of recognizing specific glycan structures and serve as invaluable tools for the ...
Proteins including glycoproteins and lectins play important roles in many biological processes. Ther...
Scheme of the affinity pull-down assay as in Fig 4. IN: sample before fractionation, UB: unbound fra...
<p>Schematic presentation of purification strategy showing various starting materials for SNA-chroma...
A: Scheme of the affinity pull-down assay. IN: sample before fractionation, UB: unbound fraction (Si...
Affinity chromatography is a method which depends essentially on the interaction between the molecul...
The work described here examines displacement phenomena that play a role in lectin affinity chromato...
<p>Dot blots of the two α-Syn-nAbs standard preparations of one IvIG batch and the affinity chromato...
<p>A. Representative LC-MS chromatograms of a IgG sepharose-binding molecule (m/z 1414.3) are shown ...
Virtually all extracellular proteins in humans are glycoproteins and likewise are many biopharmaceut...
Lectin affinity chromatography (LAC) offers a tool that aids purification of cell surface glycoconju...
<p>Comparison of the four chromatographic methods for immunoglobulin isolation that were evaluated i...
Lectins are sugar-binding proteins that can recognize and bind to carbohydrates conjugated to protei...
Lane M, Molecular Marker (Color Prestained Protein Standard, Broad Range, NEB); lane 1, culture supe...
<p>The binding of sialic acid specific lectin (MAA, <i>Maackia amurensis</i>) to A2HSG in (A) untrea...
Lectins are capable of recognizing specific glycan structures and serve as invaluable tools for the ...
Proteins including glycoproteins and lectins play important roles in many biological processes. Ther...