Digital PCR DS-100

A new nucleic acid detection and quantitative method is proposed to allocate the standard PCR reaction to a large number of tiny reactors (droplet) to achieve single-molecule template amplification and count the copy number of the target sequence by the number of positive droplet;

Absolute quantitative method, independent of standard curve and reference sample;

Compared with traditional qPCR, it has more excellent sensitivity, specificity and accuracy.

It performs well in the detection of extremely small nucleic acid samples, detection of rare mutations under complex background and identification of small differences in expression levels.

Dual fluorescence detection platform technology;

Cancer research, infectious disease detection, pharmacogenomics development, biomarker development;

Food safety and environmental monitoring;

It has wide application prospects in gene expression research, microRNA research, genome copy number identification, rare mutation detection of cancer markers, identification of pathogenic microorganisms, and identification of genetically modified components.