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Updated: May 6, 2026

Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
Published on: November 13, 2021
Development of an indirect competitive immunoassay for walnut protein component in food
Haiyan Wang1, Gang Li, Yajun Wu
1Institute of Food Safety, Chinese Academy of Inspection and Quarantine, No. 3, Gaobeidian North Road, Chaoyang District, Beijing 100123, PR China; Inner Mongolia Entry-Exit Inspection and Quarantine Bureau, No. 12, Erdos Street, Huhhot, Inner Mongolia 010020, PR China.
Abstract:
Among food allergens, walnut is a frequent cause of adverse food reactions in allergic patients. In this study, the walnut allergen protein 2S albumin precursor (Jug r 1) cDNA was synthesised and cloned into the pGEX-6P-1 expression vector. The recombinant plasmids were transformed into Escherichia coli (E. coli) BL21(DE3) pLys for expression of protein Jug r 1. Polyclonal antibodies were prepared against the expressed purified Jug r 1 protein. An indirect competitive enzyme-linked immunosorbent assay (ELISA) for the detection and quantification of walnut soluble proteins in processed foods was developed using the prepared polyclonal antibodies. The developed ELISA had a high specificity, walnut protein standard solution at 2.2 ng/mL [inhibition concentration (IC80) of the competitive test] was clearly identified by the ELISA. The mean recoveries ranged from 86% to 112%. The coefficient of variation (CV) for the 4 model foods was 6.4-8.7%.
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