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INOSeqX Series Automated Genetic Analyses / DNA Sequencers

  • All-open detection platform
  • Meet the requirements of STR analysis and gene sequencing
  • 6 patents for invention, 10 patents for utility model, 4 software copyrights
  • Fluorescence excitation efficiency 40% higher than foreign competing products
  • Solid-state laser featuring stable power and long life
  • Advanced thermal system enabling precise temperature control
  • Smaller size
  • User-friendly Windows 10 operating system and multi-language software interface

 

INOVIALAB INOSeqX Series Genetic Analyzer


The INOVIALAB INOSeqX Series is a high-performance genetic analysis platform specifically engineered for individual identification and kinship analysis within forensic DNA laboratories. As a fully all-open platform, the INOSeqX Series ensures seamless compatibility with reagent kits and consumables from leading global manufacturers, offering unparalleled flexibility in laboratory workflows.

This comprehensive ecosystem integrates precision hardware, optimized built-in reagent kits, advanced data capture software, and expert analysis tools. It is the definitive solution for handling complex forensic cases and constructing robust DNA databases with clinical-grade reliability.

 

Versatile Application Suite

 

The INOSeqX Series excels in a wide array of specialized genomic applications:

  • Fragment Analysis & Disease Linkage Mapping
  • SNP, SNPlex, and SNPshort Analysis
  • Methylation & AFLP / MLPA Analysis
  • LOH (Loss of Heterozygosity) & SSCP Analysis

 

 

 

Technical Performance & Competitive Edge


The performance benchmarks of the INOVIALAB INOSeqX Series are designed to compete with and exceed the standards of the world’s leading genetic analysis technologies:

 

Superior Reproducibility: Delivers intact, high-definition DNA typing maps for fragment analysis, consistently matching the results of industry-leading products.

 

Ultra-High Sequencing Precision: Features a standard deviation of SD ≤ 0.12bp and baseline noise of ≤ 50RFU. This level of sensitivity allows for the distinct recognition of even 1bp (base pair) differences between DNA fragments.


Real-Time Accuracy: Displays real-time peak height ratios, enabling the precise identification of heterozygote positions without data loss or oversight.

 

Phred Q20 Standardized Accuracy: Every base interpretation is validated by the Phred Q20 standard. The system achieves an impressive 900+ bp read length while maintaining a rigorous 98.5% accuracy rate.

 

TECHNICAL SPECIFICATIONS

 

Physical and Environmental Conditions


  • Dimensions: 812 mm × 610 mm × 532 mm

  • Weight: 120 kg

  • Ambient Temperature: 15-30°C (temperature fluctuation should not exceed ±2°C while working)


Power and Electrical Requirements


  • Power Supply Voltage: 220±10%V, 50 Hz ± 1 Hz

  • Current & Power: Maximum current: 10A | Maximum power: 800W (Note: This is an approximation, computers and monitors are not included)

 

Performance and Technical Parameters


  • Number of Channels: 16 (extensible)

  • Capillary Length: 36, 50, 80

  • Number of Fluorescent Dyes: 6

  • Laser Type: Long-life, high efficiency semiconductor solid-state laser

  • Laser Wavelength: 505nm

  • Resolving Power: 1bp

  • Accuracy (in the 50-400bp range): SD≤0.12bp

  • Temperature Control Accuracy: △T≤0.2°C

  • Sequencing Function: Available


Usage and Operation


  • Consumables: Self-sufficient
  • Reagents: Self-produced

  • Application Scenarios: Public security departments, medical treatment & healthcare, schools and enterprises

 


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