Simple operation
Molecular-level testing that does not require specialist staff. A two-step workflow: extract, then amplify and read.
ZC Bioscience develops RAA isothermal amplification reagents, rapid extraction kits and the portable Genchek fluorescence analyzer — so molecular testing can leave the thermal cycler behind and travel to the sample.
All reagents are for research use only. Not for use in diagnostic procedures.
Recombinase-Aided Amplification (RAA) is a rapid isothermal nucleic acid amplification technology. A recombinase obtained from bacteria or fungi binds tightly to the primer DNA at ambient temperature, forming a recombinase–primer complex. When the primer locates its fully complementary sequence on the template, single-stranded DNA-binding protein helps open the double strand, and DNA polymerase synthesises a new complementary strand. The product accumulates exponentially.
With a labelled fluorescent probe the reaction can be read in real time; a fluorescence result is typically available within 5–15 minutes. All reaction components are pre-mixed and lyophilised in the tube — add Buffer A, Buffer B and the extracted sample DNA. RAA can in principle be multiplexed: two or more primer pairs in one reaction amplify several targets simultaneously.
Molecular-level testing that does not require specialist staff. A two-step workflow: extract, then amplify and read.
Results in 5–15 minutes with a fluorescent probe; truly rapid testing for high-volume sample streams.
High sensitivity and specificity — the recombinase–primer complex recognises the target sequence by base pairing.
Compact instruments suited to harsh field conditions and on-site inspection, with battery operation on the Genchek analyzer.
Runs at 30–42 °C. No thermal cycler or other expensive equipment is required — a heat block or water bath is enough for gel readout.
Reagents supplied as freeze-dried pellets: ready to use, easy to ship, and free from freeze–thaw loss and pipetting error.
Where isothermal recombinase-driven amplification sits against the two methods most laboratories already run.
| Parameter | ● RAA | PCR | LAMP |
|---|---|---|---|
| Enzymes | Recombinase, SSB, strand-displacing DNA polymerase | Taq DNA polymerase | Strand-displacing DNA polymerase |
| Reaction temperature | 37–39 °C, constant | High temperature, thermal cycling | 60–65 °C, constant |
| Reaction time | 15 min | 1.5 h | 40 min |
| Primer pairs | 1 | 1 | 2 |
| Reagent format | Lyophilised pellet | Liquid | Liquid |
| Readout | Gel; real-time fluorescence; lateral-flow strip | Gel; real-time fluorescence | Visual turbidity |
| Noted drawback | — | Slow | Aerosol carry-over, false positives |
Every reagent below is for research use only (RUO). Pricing is by quotation — tell us your targets and volumes.

Open RAA chemistry for laboratories developing their own assays. All components are pre-mixed and lyophilised; primers should be 30–35 bp and probes 46–52 bp for optimal performance. Fluorescent kits use a probe cleaved by exonuclease for real-time readout; RT kits reverse-transcribe RNA first.
Rapid amplification of DNA at 37 °C; product confirmed by agarose gel electrophoresis. Runs on a heat block, water bath or incubator.
Rapid amplification of DNA with real-time monitoring on the Genchek analyzer or a standard real-time PCR instrument; 5–20 min.
Rapid amplification of RNA; reverse transcription then isothermal amplification at 37 °C with gel readout.
Rapid amplification of RNA with real-time fluorescence readout on Genchek or qPCR instruments; 5–20 min.
Rapid DNA amplification at 39 °C; a dual-labelled amplicon is read on a universal nucleic acid lateral-flow strip — no instrument needed.
Rapid RNA amplification at 42 °C with lateral-flow strip readout; reverse transcription built in.

An integrated, portable rapid-test analyzer for on-site and mobile testing. Built-in reagent mixing, fully matched to RAA reagents; dual fluorescence channels (FAM & ROX); automatic data analysis and report generation with multiple report-export options. All assays run under one software interface and results are read from a single display.
| Throughput | 8 wells × 2 channels — up to 16 targets per run |
|---|---|
| Fluorescence channels | FAM / ROX |
| Temperature range · accuracy | Ambient to 65 °C · ±0.5 °C |
| Net weight · dimensions | 3.8 kg · 255 × 240 × 123 mm |
| Power | 120 W · AC 100–240 V, 50/60 Hz |
| Operating environment | 5–35 °C, 20–80 % RH |

Purpose-built front ends for the RAA reaction: heat-lysis, spin-column and magnetic-bead formats that yield amplification-ready DNA or RNA without hazardous solvents and with low cross-contamination risk.
Genomic DNA in 5 minutes from animal tissue, blood, meat products, plant tissue, seeds and bacteria. A surfactant lysis mix with no protein or RNA removal steps.
Lyse–bind–wash–elute in 15 minutes. Animal tissue, cells, bacteria, saliva, blood, swabs, faeces, bone and feed; high yield and stable quality.
Four steps, 10 minutes, high-quality RNA from animal tissue, cells, saliva, blood, swabs and faeces — ready for RT-RAA.
For automated magnetic-bead extractors. Nano-magnetic-bead purification of DNA from animal tissue, cells, saliva, blood and swabs in 25 minutes; cuts hands-on time for large sample batches in food safety, environmental microbiology, livestock and molecular biology research.

Target-specific kits that recognise and amplify a species- or pathogen-specific gene fragment at 30–42 °C (optimum 37–39 °C). Result read directly from the amplification curve and time — no electrophoresis.
Species-specific kits for animal tissue, blood, foods, meat products (including processed meat) and feed. No cross-reaction observed between the listed species; different breeds of each species are detected.
Qualitative detection in foods, beverages, water, cosmetics, disposable hygiene products and seafood; result in 5–15 min. Method reference: GB 4789 series and SN/T standards for each organism.
Element kits for the six common screening elements, plus event-specific kits for GM soybean, maize and canola lines listed in our catalog. 24 tests per kit.
Fully automated, sample-in / result-out in 30 minutes. Performs quantitative pipetting, sample lysis, nucleic acid purification, isothermal amplification, fluorescence detection, analysis and reporting in one instrument — load the sample and the system does the rest.
| Run time | ~30 min, extraction and amplification integrated |
|---|---|
| Sample throughput | 1 sample per run |
| Fluorescence channels | FAM / ROX |
| Interface | 7-inch colour touchscreen |
| UV lamp · air purification | Yes · Yes |
| Weight · dimensions | 16 kg · 260 × 325 × 420 mm |
| Power | 221 W · AC 220 V, 50 Hz |
| Pipetting | <15 µL accuracy >98 %, CV <5 %; 15–50 µL >98.5 %, CV <3 %; >50 µL >99 %, CV <1.2 % |
Each solution pairs target-specific RAA fluorescent kits with the Genchek analyzer, which monitors amplification in real time and completes the run in 15 minutes.

As price gaps between meats widen, species substitution and adulteration are increasingly common. RAA-based species kits detect species-specific genes, identifying meat origin at the molecular level with no cross-reaction between species.
For regulators, customs and border inspection, livestock authorities, agricultural research institutes; food, dietary-supplement and feed manufacturers; third-party testing laboratories.

In China, pathogenic bacteria account for an estimated 40–50 % of reported foodborne-illness cases each year. RAA pathogen kits combine multi-channel detection, short run times and high sensitivity — raising throughput and moving food-safety warnings earlier.
Qualitative detection in food, beverages, cosmetics and seafood. Method reference: GB 4789 series, SN/T. For regulators, public-health laboratories, food and cosmetics manufacturers, third-party laboratories.

GM crops carry genes introduced from other organisms to alter traits, nutrition or quality, and regulators worldwide require labelling and control. RAA-based GMO kits specifically detect exogenous elements and events in crops, identifying GM material at the molecular level.
For regulators, customs and border inspection, agricultural research institutes; food and feed manufacturers; third-party testing laboratories.
Consultation, documentation, training and after-sales support from the team that develops the chemistry — plus custom assay development for targets not yet in the catalog.
Our R&D team answers every product question with patient explanation and demonstration. Example workflow for a species assay: weigh 50 mg sample into the extraction solution, incubate at 70 °C for 10 min; add 45.5 µL Buffer A, 2.5 µL Buffer B and 2 µL template; place in the Genchek analyzer; result in 5–15 min.
Good after-sales service earns customer trust. We provide quality after-sales support with long-term technical documentation. Our engineers respond promptly and resolve issues remotely by email, online session or phone.
RAA is a versatile, portable rapid-testing platform that can replace LAMP or PCR in many workflows. We develop custom RAA assays on request and co-develop detection kits with partner organisations under strategic agreements.
Hangzhou ZC Bio-Sci & Tech Co., Ltd. ("ZC Bioscience") develops and applies Recombinase-Aided Amplification (RAA), an isothermal nucleic acid amplification technology, and supplies RAA-based reagents, extraction kits and portable fluorescence instruments for rapid molecular testing.
Since September 2016 the company has accelerated product development for RAA-based rapid food-safety testing, launching in turn the animal-species molecular detection series, the foodborne pathogen molecular detection series and the GMO ingredient molecular detection series. ZC Bioscience has signed strategic cooperation agreements with government institutions and research organisations across several fields to co-develop RAA-based detection kits.





In vitro nucleic acid amplification lets trace amounts of nucleic acid be amplified rapidly and efficiently. RAA is an isothermal method built on existing amplification principles: recombinase, single-stranded DNA-binding protein and DNA polymerase replace the thermal-cycling denaturation of conventional PCR, so amplification proceeds at a constant 37 °C.
On 20–22 July 2017 the 7th Food Microbiology Detection and Control Technology Exchange was held in Shanghai, jointly organised by the Agro-product Safety Research Center of the Chinese Academy of Inspection and Quarantine, the Analytical Microbiology Committee of the Chinese Society for Microbiology, and Foodmate. The meeting ran 17 themed sessions with over 30 exhibitors and 300+ laboratory professionals.
Foodborne disease caused by pathogenic microorganisms is the number-one food-safety issue. Controlling contamination, strengthening laboratory capability and applying advanced microbial detection and control technology in production have become focal concerns for regulators and food companies alike. ZC Bioscience will attend and exhibit.
The annual CBIFS food-safety technology forum was held on 7–8 April 2017 at the Hangzhou International Expo Center. ZC Bioscience, a newcomer to food-safety testing, made its debut at the conference; on the morning of the 7th the ZC Bioscience booth drew strong visitor interest.
Send us your targets, sample types and monthly volumes. We reply with a quotation, instructions for use and compatible-instrument guidance.