Abstract
Indirect enzyme-linked immunosorbent assays (ELISA) technique was used to identify and quantify the use of dried egg white (DEW) and whey protein concentrate (WPC) in crabsticks. The use of SDS-PAGE for the quantification of protein additives has had limited success due to the high shear and high temperature processes of surimi crabstick. Monoclonal (anti-heat-denatured ovalbumin) and polyclonal (anti-β-lactoglobulin) antibodies were used. Antibodies showed no significant cross-reactivity with non-target crabstick proteins. An optimised extraction solution of 10% SDS and 2.5% 2-ME yielded high extractability with improved consistency. Quantification of DEW and WPC was achieved using the optimised extraction solution and indirect ELISA. Estimated DEW values were within 7% of actual values, WPC samples were within 17%. Inter-assay coefficients of variance for DEW ranged from 0.9% to 3.1% and those of the WPC were 1.0-8.0%.
Original language | English |
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Pages (from-to) | 575-581 |
Number of pages | 7 |
Journal | Food Chemistry |
Volume | 118 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2010 Feb 1 |
Keywords
- Antibody
- Dried egg white
- ELISA
- Quantification
- Whey protein concentrate
ASJC Scopus subject areas
- Analytical Chemistry
- Food Science