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Related Concept Videos

Affinity Chromatography01:03

Affinity Chromatography

Affinity chromatography is a powerful technique extensively utilized for separating and purifying specific biomolecules from complex mixtures. It capitalizes on the highly selective binding between an analyte and its counterpart, such as antibody-antigen interactions. The counterpart is immobilized on the stationary phase, forming an affinity column. The stationary phase typically consists of solid support, such as agarose or porous glass beads, immobilizing the affinity ligand. The mobile...
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
Types Of Column Chromatography01:29

Types Of Column Chromatography

The stability and compatibility of column material with samples are crucial for efficient purification in chromatographic techniques. Various operating parameters such as pH, temperature, or solvent affect the packing of the column material, thereby determining the purification efficiency. The choice of column material also plays an essential role in deciding the operating parameters and can be modified based on the proteins that need to be purified.
Gel Filtration Chromatography
When the...
Silica Gel Column Chromatography: Overview01:10

Silica Gel Column Chromatography: Overview

Silica gel column chromatography is a technique for separating compounds using a column packed with silica gel as the stationary phase. This method relies on differences in the polarity of compounds. Based on their polarities, compounds move between the stationary phase (silica gel) and the mobile phase (the solvent), forming discrete bands in the column.
Polar components tend to bind strongly to the silica gel, causing them to move slowly through the column. In contrast, nonpolar compounds...

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Updated: Jun 16, 2026

Activated Cross-linked Agarose for the Rapid Development of Affinity Chromatography Resins - Antibody Capture as a Case Study
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Bioaffinity chromatography on monolithic supports.

Kishore K R Tetala1, Teris A van Beek

  • 1Laboratory of Organic Chemistry, Natural Products Chemistry Group, Wageningen University, Wageningen, The Netherlands. kishore.tetala@gmail.com

Journal of Separation Science
|January 26, 2010
PubMed
Summary

This review highlights monolithic materials for bioaffinity chromatography, enabling rapid analysis and biomarker enrichment. Recent research showcases diverse ligands and applications, with epoxy CIM disks being the most utilized format.

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Published on: January 8, 2014

Area of Science:

  • Analytical Chemistry
  • Biochemistry

Background:

  • Affinity chromatography on monolithic supports offers fast analyses, small sample volumes, and strong enrichment of trace biomarkers.
  • Monolithic materials are increasingly used in bioaffinity chromatography, including immunochromatography, for analytical and preparative applications.

Purpose of the Study:

  • To review recent research on monolithic materials in bioaffinity chromatography.
  • To discuss biomolecules used as ligands, monolith preparation, formats, and applications.

Main Methods:

  • Review of recent scientific literature (37 papers in the last four years).
  • Discussion of various biomolecules (antibodies, enzymes, lectins, aptamers) as ligands.
  • Exploration of monolith preparation, formats (disks, capillaries, microchips), and ligand immobilization.

Main Results:

  • Protein A and G remain primary ligands for immunoglobulin enrichment.
  • Antibodies and lectins are popular for analyzing smaller molecules and saccharides.
  • Cryogels with ligands are used for cell and bacteria sorting; aptamers and phages are new ligand applications.
  • Convective interaction media (epoxy CIM disks) are the most common format.

Conclusions:

  • Monolithic bioaffinity chromatography is a powerful analytical platform with diverse and evolving applications.
  • The choice of ligand and monolith format depends on the target analyte, with established ligands still dominant but new ones emerging.