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Updated: Jun 19, 2026

An Economical and Versatile High-Throughput Protein Purification System Using a Multi-Column Plate Adapter
Published on: May 21, 2021
Inexpensive synthetic-based matrix for both conventional and rapid purification of protein A- and tandem affinity
Kenneth E Sawin1, Claudia C Bicho, Hilary A Snaith
1Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, UK. ken.sawin@ed.ac.uk
Abstract:
Immunoglobulin G (IgG)-Sepharose is often used for purification of protein A- and tandem affinity purification (TAP)-tagged proteins from eukaryotic cells, but because it is based on an agarose matrix, it is not always optimal for all proteins. Synthetic matrices such as IgG-Dynabeads have improved properties over IgG-Sepharose but are generally expensive. Here we describe the preparation and properties of an IgG matrix based on Fractogel EMD beads. As a synthetic-based matrix, IgG-Fractogel has clear advantages over IgG-Sepharose. IgG-Fractogel can also be used in applications that usually use IgG-Dynabeads but at a significantly reduced cost.
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