

Food Allergen ELISA Microplate System
食品过敏原 ELISA 微孔板系统
- SKU FSA-0004
- Food Safety Analysis
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- AOAC performance-tested kit (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Assay format | Sandwich ELISA, 96-well |
|---|---|
| Detection wavelength | 450 nm with 620 nm reference |
| Detection limits | 1–10 mg/kg per allergen |
| Quantification range | 2–40 mg/kg (typical) |
| Extraction time | 15–30 min |
| Total assay time | 60–120 min |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO/IEC 17025, AOAC Official Methods of Analysis, EN 15633-1
What is the Food Allergen ELISA Microplate System?
A food allergen ELISA microplate system quantifies specific allergenic proteins in ingredients, finished products and cleaning swabs using antibody-based colorimetric assays. It provides the sensitive, quantitative verification needed for allergen labelling and cleaning validation.
What is the Food Allergen ELISA Microplate System?
A food allergen ELISA microplate system quantifies specific allergenic proteins in ingredients, finished products and cleaning swabs using antibody-based colorimetric assays. It provides the sensitive, quantitative verification needed for allergen labelling and cleaning validation.
Overview
The assay uses a sandwich format in which capture antibodies bound to a microplate well bind the target allergen, and a second enzyme-labelled antibody produces a colour proportional to concentration after substrate addition. Absorbance is read at 450 nm with a reference wavelength, and concentrations are interpolated from a calibration curve. Kits are available for gluten, milk, egg, soy, peanut, hazelnut, almond, sesame, shellfish, mustard, celery and lupin, with detection limits commonly between 1 and 10 mg/kg. Sample preparation involves extraction in a supplied buffer, centrifugation and dilution, and results are reported in mg/kg of food. The method is suitable for screening and cleaning verification, with confirmation by a second technique for label decisions.
How does it work?
Food safety analysis separates the analyte from the food matrix and then quantifies it with a detector matched to its chemistry. High-performance liquid chromatography suits non-volatile additives, sweeteners and preservatives, with UV or diode-array detection and confirmation by mass spectrometry. LC-MS/MS gives the sensitivity and selectivity needed for pesticide residues at microgram per kilogram levels. Gas chromatography with mass detection covers volatile compounds such as solvents, flavours and some pesticide classes. Immunoassays rely on antibodies that bind allergens or toxins, producing a colorimetric signal proportional to concentration. PCR amplifies species-specific DNA sequences to identify allergens or adulterants. Rapid screening kits are confirmed by instrumental methods when a result is positive or disputed.
What are the key features?
- Quantitative sandwich ELISA with 96-well microplate format
- Kit panels for gluten, milk, egg, soy, peanut and tree nuts
- Detection limits typically 1–10 mg/kg of food
- Single extraction protocol across the allergen panel
- Microplate reader compatibility at 450 nm
- Cleaning-swab protocols for production-line verification
What are the technical specifications?
A typical food allergen elisa microplate system configuration offers assay format of Sandwich ELISA, 96-well, detection wavelength of 450 nm with 620 nm reference, detection limits of 1–10 mg/kg per allergen, quantification range of 2–40 mg/kg (typical), extraction time of 15–30 min and total assay time of 60–120 min. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Food Allergen ELISA Microplate System is used in allergen labelling verification, cleaning validation for shared production lines, incoming ingredient screening and investigation of consumer allergen complaints. Across the wider Food Safety Analysis class, laboratories also deploy it for pesticide residue monitoring in fruit and vegetables, additive and preservative limit checks and allergen verification and cleaning validation.
Which standards and certifications apply?
Relevant standards and methods include ISO/IEC 17025, AOAC Official Methods of Analysis, EN 15633-1, EN 15634-1, Regulation (EC) No 396/2005, SANTE/11312/2021 and Codex Alimentarius. Certification candidates for this model are CE, ISO 9001 manufacturing and AOAC performance-tested kit; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Food matrices vary widely, so method validation must cover each commodity group, including fatty, acidic and high-pigment samples that cause ion suppression or interference. Standard solutions, antibodies and enzyme kits have limited shelf life and need controlled storage. Laboratories should participate in proficiency testing and keep traceable records of calibrations, control charts and confirmatory analysis. Allergen testing demands strict cleaning and segregation to avoid cross-contamination between samples. Confirm that your chosen platform has local service, spare parts and consumables, and that software meets data-integrity requirements when results support regulatory decisions.
How do I select the right Food Allergen ELISA Microplate System?
Select an ELISA allergen system when you need quantitative screening and cleaning verification for a defined allergen panel. Confirm that validated kits exist for each allergen and matrix you test, since cross-reactivity and recovery vary. Compare detection limits with the labelling thresholds that apply, and specify reader compatibility and software for control charts.
How does it compare with other Food Safety Analysis variants?
Match the detection technology to the analyte and to the limit you must reach. HPLC with UV or diode-array detection is sufficient and economical for many additives and preservatives at milligram per kilogram levels. Pesticide residue work at microgram per kilogram levels requires LC-MS/MS or GC-MS/MS, and multi-residue methods should cover the classes in your monitoring plan. Choose ELISA or lateral-flow kits when speed, low cost and on-site use matter, accepting them as screening tests. Real-time PCR is required for species identification and authenticity claims. Confirm the availability of certified reference standards, matrix-matched calibration and validated methods for your specific commodities.
Full specifications
| Assay format | Sandwich ELISA, 96-well |
|---|---|
| Detection wavelength | 450 nm with 620 nm reference |
| Detection limits | 1–10 mg/kg per allergen |
| Quantification range | 2–40 mg/kg (typical) |
| Extraction time | 15–30 min |
| Total assay time | 60–120 min |
| Allergen panel | Gluten, milk, egg, soy, peanut, tree nuts |
| Sample types | Food, rinse water, swabs |
| Storage | 2–8 °C for kits and standards |
| Reader interface | USB, spreadsheet export |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Allergen labelling verification
- Cleaning validation for shared production lines
- Incoming ingredient screening
- Investigation of consumer allergen complaints
Key features
- Quantitative sandwich ELISA with 96-well microplate format
- Kit panels for gluten, milk, egg, soy, peanut and tree nuts
- Detection limits typically 1–10 mg/kg of food
- Single extraction protocol across the allergen panel
- Microplate reader compatibility at 450 nm
- Cleaning-swab protocols for production-line verification
Frequently asked questions about Food Allergen ELISA Microplate System
Capture antibodies on the plate bind the target protein, then a second enzyme-labelled antibody attaches and converts a substrate to a coloured product. Absorbance at 450 nm is proportional to allergen concentration and is read against a calibration curve.
Results are reported as milligrams of allergenic protein per kilogram of food for the specific allergen tested. They are method and kit specific, so results from different kits should not be compared directly without demonstrating equivalence.
Yes. Swabs or rinse water from production surfaces are analysed with the same kits, and results are compared with an internal action limit. Cleaning validation usually combines ELISA with visual inspection and, for critical allergens, a confirmatory method.
Typical targets are pesticide residues, veterinary drug residues, additives and preservatives, allergens, mycotoxins, illegal dyes, heavy metals and adulterants. The exact panel depends on the commodity, the country of sale and the monitoring plan of the competent authority.
LC-MS/MS is used for most polar and semi-polar pesticides, and GC-MS/MS for volatile and non-polar compounds. Multi-residue methods based on QuEChERS extraction cover several hundred analytes in one run, with isotope-labelled internal standards correcting for matrix effects.
ELISA is widely used for allergen screening and cleaning verification because it is sensitive and simple, but positive results and label decisions are usually confirmed by a second method, and quantitative reporting requires proper validation for each matrix.
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