

Real-Time PCR System for Food Authenticity Testing
食品真伪检测实时荧光 PCR 系统
- SKU FSA-0006
- Food Safety Analysis
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Optical channels | 4–6 fluorescence channels |
|---|---|
| Sample capacity | 96-well or 48-well block |
| Temperature uniformity | ±0.3 °C |
| Heating rate | Up to 5 °C/s |
| Detection limit | 0.1 percent species content |
| Run time | 40 cycles in 45–60 min |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO/IEC 17025, AOAC Official Methods of Analysis, EN 15633-1
What is the Real-Time PCR System for Food Authenticity Testing?
A real-time PCR system for food authenticity identifies species and detects adulteration by amplifying species-specific DNA sequences and reading fluorescence in each cycle. It supports meat species verification, GMO screening and label-claim validation.
What is the Real-Time PCR System for Food Authenticity Testing?
A real-time PCR system for food authenticity identifies species and detects adulteration by amplifying species-specific DNA sequences and reading fluorescence in each cycle. It supports meat species verification, GMO screening and label-claim validation.
Overview
DNA is extracted from the food sample, and target sequences are amplified with species-specific primers and a fluorescent probe. Fluorescence increases with each cycle in proportion to the starting copy number, and the cycle threshold value indicates whether the target is present and, with a standard curve, how much. The technique detects very low levels of a species even in processed and heat-treated products, and melting-curve analysis or multiplexed dyes allow several targets in one reaction. Quantitative assays estimate the percentage of a species in a mixture, while qualitative assays answer presence or absence. Dedicated food authenticity kits cover beef, pork, poultry, horse, fish species, soybean, GMO events and allergens, with detection as low as 0.1 percent.
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?
- Real-time fluorescence detection across four to six channels
- Species-specific kits for meat, fish, plant and GMO targets
- Quantification down to about 0.1 percent species content
- Melting-curve analysis for multiplex confirmation
- Fast cycling with 40 cycles in under 60 minutes
- Audit-trail software with plate setup and result reporting
What are the technical specifications?
A typical real-time pcr system for food authenticity testing configuration offers optical channels of 4–6 fluorescence channels, sample capacity of 96-well or 48-well block, temperature uniformity of ±0.3 °C, heating rate of Up to 5 °C/s, detection limit of 0.1 percent species content and run time of 40 cycles in 45–60 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 Real-Time PCR System for Food Authenticity Testing is used in meat and fish species verification, GMO screening and labelling compliance, detection of undeclared plant or animal material and halal and kosher claim verification. 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 and ISO 9001 manufacturing; 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 Real-Time PCR System for Food Authenticity Testing?
Choose a real-time PCR system when authenticity claims, species identity or GMO status must be demonstrated. Confirm the availability of validated kits for your commodities and the number of fluorescence channels needed for multiplex assays. Consider DNA extraction automation, contamination controls and software that supports audit trails if results are used in regulatory or contractual disputes.
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
| Optical channels | 4–6 fluorescence channels |
|---|---|
| Sample capacity | 96-well or 48-well block |
| Temperature uniformity | ±0.3 °C |
| Heating rate | Up to 5 °C/s |
| Detection limit | 0.1 percent species content |
| Run time | 40 cycles in 45–60 min |
| Dyed multiplexing | FAM, HEX, ROX, Cy5 |
| Consumables | 96-well plates, strip tubes |
| Software | Quantitation, melt curve, audit trail |
| Data export | CSV, PDF, LIMS export |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Meat and fish species verification
- GMO screening and labelling compliance
- Detection of undeclared plant or animal material
- Halal and kosher claim verification
Key features
- Real-time fluorescence detection across four to six channels
- Species-specific kits for meat, fish, plant and GMO targets
- Quantification down to about 0.1 percent species content
- Melting-curve analysis for multiplex confirmation
- Fast cycling with 40 cycles in under 60 minutes
- Audit-trail software with plate setup and result reporting
Frequently asked questions about Real-Time PCR System for Food Authenticity Testing
Primers and probes target DNA sequences unique to a species or event, so amplification proves that material is present even in processed food. With a standard curve, the amount of target DNA can be related to the percentage of that species in the mixture.
Yes, within limits. Quantitative real-time PCR compares sample signals with standards of known content, but DNA degradation, different tissue composition and processing can bias the result, so reported percentages carry a wider uncertainty than qualitative calls.
DNA is present in most tissues, survives many processing steps and contains species-specific sequences, so it can indicate the origin of a product even after heating or mixing. It complements protein-based methods that may fail after denaturation.
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.
Related models






