The VPCIR Technology
VPCIRTM stands for Viability Polymerase Circle Reaction. It is based on the principle of detection of enzymatic processes allowing quantification of the activity of specific DNA-modifying enzymes. This is done by providing a substrate that the DNA modifying enzyme recognize and either directly or via additional enzymes turn into a circle which subsequently are amplified and visualized. The technology may be used for various purposes such as drug screening, cancer research, or for detection of pathogens.
Enzymes are biomolecules catalyzing specific biochemical reactions. Thus, the biological relevance depends on the ability to catalyze these reactions, id est, the activity of the enzymes. Unlike PCR and ELISA methods, each target enzyme can convert many DNA substrate molecules into detectable DNA product molecules up to 500-1,000 conversions per target enzyme. Thus, the sensitivity is greatly increased both through the inherent target enzyme catalyzed conversion of substrates to products and through a subsequent isothermal amplification reaction of the generated products.
The patent pending VPCIRTM technology is based on the knowledge from more than 10 years of research in specific sensor-based assays and more than 20 years of research in DNA modifying enzymes within the VPCIR founder team. The technology is robust and capable of accurate measurements using various inputs such as recombinant enzymes for drug screening, crude cell extract as well as tissue extract for biological and anti-cancer research, blood or saliva for pathogen detection, and food-borne bacteria detected within complex food matrices as milk and meat. The technology behind is sensitive enough to detect single cells and can easily be adapted to detect multiple pathogens (multiplexed).
Uses and Users
VPCIR ™ technology is utilized in several core technology platforms:
- VPCIR ™ REEAD
- VPCIR ™ EAD
- VPCIR ™ IAD
- VPCIR ™ Enzymes
Each with different uses and users.
See detail on each technology in subsequent tabs in the menu on top.