Stronger
Higher Throughput: Supports 24 samples per run
More Fluorescent Channels: 4/5/6/(6+1) channels (FAM, HEX (VIC), ROX, Cy5, Quasar705, Atto425, with customizable channel)
Greater Multiplexity: Exponential Ultra-Multiplex Digital PCR Technology enables up to 63-plex quantitative detection
Smarter: AI-assisted chip reading and automated noise removal based on neural network algorithms
Faster
Sample Loading Time: <4 minutes
Reading Speed: Single-channel scanning time <0.5 minutes per sample Detection Speed: Total experimental process time ≤2 hours, including droplet generation, PCR amplification, and data reading and analysis More Flexible Amplification Capability: Dual PCR thermal modules for simultaneous operation of different programs Compact Design: With a width of only 440mm, it occupies minimal bench space Retains the Core Advantages of SCI Digital All-in-1, fully automated: Samples in, results out, with no manual sample loading or transfer Extensive reagent compatibility: Widely compatible with market PCR Mix, simplifying assay development. Ultimately low cost: Price comparable to qPCR; low cost per run. Superb flexibility: 2-24 samples, 1 chip/sample, minimum 2 samples/run – farewell to sample pooling, minimizing consumable waste. High performance: Sensitivity of 0.01%. Extremely easy to use: Experiment preparation can be completed in as little as 1 minute, greatly enhancing efficiency Data analysis: The software automatically performs fluorescence signal statistical analysis for each channel, calculating the initial copy number or concentration (copies/μL) of the target molecules in each sample, copy number variation (CNV), and results can be directly printed or imported into Excel. The analysis threshold line of the data analysis software can be manually adjusted, and pairwise comparisons between channels can be made. The results can be displayed through 1-D graphs, 2-D graphs, histograms, and original chip images. Innovative glass-based microfluidic chip Principal: glass-based sandwich design enabling the solidified oil isolation technology, which forms micro-droplets sealed in independent microchambers by solidifying the oil phase. A totally different approach than oil encapsulated water droplet partitioning method or flow cytometry detection principle. Advantages: prevents droplet fusion or uneven droplet sizes, ensuring more stable droplets. Rapid generation of 20,000+ droplets with higher effective droplet ratio (>95%) and droplet uniformity (>99%). Higher thermal efficiency, more uniform reactions, increased transparency for higher signal quality.
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