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Printed Glycan Array: A Sensitive Technique for the Analysis of the Repertoire of Circulating Anti-carbohydrate Antibodies in Small Animals
Published on: February 14, 2019
Solid Phase Immunoassay for the Detection of Anti-β2 Glycoprotein I Antibodies
Rohan Willis1, Elizabeth Papalardo2, E Nigel Harris3
1Antiphospholipid Standardization Laboratory, Division of Rheumatology, Department of Internal Medicine, University of Texas Medical Branch, 301 University Blvd., Galveston, TX, 77555-0883, USA. rowillis@utmb.edu.
Abstract:
The discovery in the 1990s that the protein beta-2-glycoprotein I (β2GPI) was an antigen of central importance in the antiphospholipid syndrome (APS) was soon followed by the development of ELISA assays capable of identifying anti-β2GPI antibodies recognizing this antigen. The determination of these antibodies has continued to play a major role in the management of APS patients because of their extremely high specificity for diagnosing the disease, despite their relatively poor sensitivity compared to anticardiolipin antibodies. Additionally, there is abundant evidence of the pathogenic capacity of these antibodies. In this chapter we outline the procedure for producing essential assay components and for performing the anti-β2GPI ELISA, which can be used to determine the presence of IgG, IgM and IgA anti-β2GPI antibodies in human samples. We also provide general guidelines that will facilitate optimal performance of the anti-β2GPI ELISA assay.

