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ELISA kit for determination of egg white proteins: interlaboratory study
Kvìta Tomková1, Petr Cuhra, Jana Rysová
1SEDIUM RD, Ltd, Zelezniènìho pluku 1361, 530 02 Pardubice, Czech Republic.
Journal of AOAC International
|February 15, 2011
Summary
This study validated an ELISA method for quantifying egg white proteins (EWPs) in foods. The validated ELISA kit demonstrated high specificity and reliability across diverse food matrices.
Area of Science:
- Food science
- Analytical chemistry
- Immunology
Background:
- Accurate quantification of egg white proteins (EWPs) is crucial for food safety and labeling.
- Existing methods may lack specificity or be unsuitable for complex food matrices.
- Development of a reliable method for EWP detection is needed.
Purpose of the Study:
- To validate an Enzyme-Linked Immunosorbent Assay (ELISA) method for the quantitative determination of EWPs in various food products.
- To assess the performance of the ELISA kit across multiple laboratories and diverse food matrices.
Main Methods:
- An interlaboratory study involving 11 laboratories.
- Utilized an ELISA kit based on sheep polyclonal antibodies for EWP quantification.
- Tested 10 food samples, including matrices with and without EWPs.
- Statistical analysis including ANOVA, Cochran, Dixon, and Mandel tests were employed.
Main Results:
- The ELISA kit showed no false-positive results or cross-reactivity in a broad range of food matrices.
- Limit of Quantification (LOQ) was determined to be 1.4 mg EWP/kg, and Limit of Detection (LOD) was 0.43 mg EWP/kg.
- The method proved reliable for detecting EWPs in food samples, with high agreement among laboratories.
Conclusions:
- The validated ELISA method is suitable for the accurate and reliable quantification of EWPs in foods.
- The kit's specificity and sensitivity make it a valuable tool for food analysis and allergen detection.
- The interlaboratory study confirmed the robustness of the ELISA method for routine food testing.
