Single thermal protocol
The same thermal cycle across the kit family. DNA or RNA target makes no difference — the user does not set up a new protocol for each kit.
→ Multiple kits in parallel on the same instrument, no protocol changes.
The next-generation platform for molecular diagnostics.
We translate multiplex real-time PCR technology into the clinical laboratory workflow. A single thermal protocol, a single standard, a consistent user experience across the kit family — integrated digital diagnostic flow with companion software.
Uniqplex designs multiplex real-time PCR as a platform — a single thermal cycle, a single positive control, the same user experience across every Ant Biotech kit. The eight points below are the concrete differences that set the lab workflow apart from ordinary PCR.
The same thermal cycle across the kit family. DNA or RNA target makes no difference — the user does not set up a new protocol for each kit.
→ Multiple kits in parallel on the same instrument, no protocol changes.
A single positive control formula applies to all kits. There is no need to keep a separate PC stock for each kit or to track separate expiry dates.
→ Streamlined consumable management, simple cold chain.
With the UMS plate editor you can define samples from different kits on the same plate and process them in a single run. No need to batch samples.
→ Patients don't wait for results, the lab leaves no empty wells.
In quantitative kits the standard curve is generated automatically and the copies/mL result is reported in a single click. No manual formula entry.
→ No calculation errors, no transcription errors.
Serial results from the same patient are tracked together; the viral load trend is shown as a graph. A single screen for transplant follow-up and antiviral response.
→ One patient, many time points, one window.
Even in qualitative kits, UMS converts the Cq value into "high / medium / low load" categories. The clinician receives information beyond positive/negative.
→ A single detection, more clinical decisions.
Kit reagents arrive ready in a snap-off plate format. No pre-mixing, aliquoting or calculations — add the sample and run.
→ Fewer user errors, shorter set-up time.
An internal control co-amplified in every well on the HEX channel — β-Globin or RNase P. Extraction success, presence of cellular material and PCR inhibition are verified automatically.
→ Minimal false-negative risk, validation in every reaction.
All kits run on the same Uniqplex platform; the clinician selects a category based on the answer being sought in the sample.
COVID-19, Influenza, RSV, Adenovirus and broad respiratory panels.
Diarrhea pathogens and C. difficile detection panels.
STI panel, HPV genotyping family, HSV quantification.
Meningitis and encephalitis panel — bacteria, viruses, fungi included.
EBV, BKV, JCV, Parvovirus B19 — transplant and immunosuppressed patients.
Aspergillus, Candida, Pneumocystis jirovecii detection.
Streptococcus pyogenes detection and monitoring.
Next-generation sequencing kits and software — under R&D.
Coming Soon
Absolute quantification kits and analysis software — under R&D.
Coming Soon
The Uniqplex kit family is in the (EU) 2017/746 IVDR conformity assessment process. A written agreement has been signed with SGS Belgium NV (Notified Body NB 1639) per IVDR Annex VII Section 4.3, and the formal application has been completed.
Under (EU) 2024/1860 transition provisions, kit supply and clinical use continue uninterrupted — clinical laboratories may safely continue using their existing Uniqplex kits. After full IVDR-CE certification, kit labels and documentation update automatically.
Reference: CLNB1639 · TR/IST/22215599 · 30 March 2026