AirPOC technology

AirPOC amplification is asynchronous PCR reaction, without the necessity for temperature cycling. By establishing a temperature gradient within a closed space, differential fluid density is formed, inducing continuous cycling of PCR reactants in different temperature zones.

Compared to traditional synchronous PCR amplification reactions, AirPOC amplification requires neither complex temperature cycling steps nor intricate and precise temperature control. Thus, significantly reduces reaction time, enabling efficient and rapid PCR amplification.

Intag high-efficiency polymerase, specifically developed for the AirPOC amplification, boasts proprietary intellectual property. Its synthesis speed surpasses that of traditional high-speed PCR polymerases, effectively enhancing amplification efficiency and enabling single-molecule amplification.

Designed for point-of-care testing (POCT) scenarios, The resilience and capacity to withstand interference of AirPOC amplification enable the direct detection of a diverse range of sample types, such as saliva and swab samples.

A patented component for the modification of primers and probes, it closes off the 3' end of primers, effectively preventing non-specific amplification and enhancing the specificity of detection for authentic samples.

The independently designed highly integrated detection module condenses complex temperature control systems and light signal detection systems onto the palm of your hand.

Based on high-performance LED lights and highly sensitive PD (photodiode) components, the light signal detection system achieves a significant improvement in fluorescence signal detection sensitivity while substantially reducing non-target fluorescence signals, enabling highly sensitive and accurate detection.