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Updated: Aug 20, 2026

Activated Cross-linked Agarose for the Rapid Development of Affinity Chromatography Resins - Antibody Capture as a Case Study
Published on: August 16, 2019
Optimised affinity purification of polyclonal antibodies from hyper immunised ovine serum using a synthetic Protein A
Anthony R Newcombe1, Chrissie Cresswell, Susannah Davies
1Process Development Group, Protherics Ltd., Blaenwaun, Ffostrasol, Llandysul, Wales SA44 5JT, UK. tony.newcombe@protherics.com
Abstract:
This report describes the applicability of a synthetic chromatography adsorbent for large-scale purification of polyclonal immunoglobulin G from hyper immunised ovine serum. Under optimised conditions, MAbsorbent A2P was shown to bind approximately 27 mg mL(-1) of ovine immunoglobulin from undiluted serum, with eluted IgG purities of >95%, minor levels of albumin (approximately 1%) and undetectable levels of leached ligand in the purified preparations. The results presented here indicate that the optimised affinity capture of immunoglobulin from ovine serum using MAbsorbent A2P is a feasible alternative to Protein A chromatography or sodium sulphate precipitation for the initial capture of antibodies from undiluted serum.
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