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TIANLONG Gentier Mini / Mini+ Portable Real-Time Fluorescent Quantitative PCR System

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Brand TIANLONG
Origin Shaanxi, China
Manufacturer Type Direct Manufacturer
Regional Classification Domestic (China)
Model Gentier Mini / Mini+
Instrument Type Real-Time Fluorescent Quantitative PCR System
Sample Throughput 16 wells
Interchangeable Thermal Block No
Effective Reaction Volume Range 0–100 µL
Max Heating Rate 5.0 °C/s
Max Cooling Rate 4.0 °C/s
Temperature Accuracy ≤ ±0.1 °C
Well-to-Well Temperature Uniformity ±0.2 °C
Detection Channels 4
Light Source High-Efficiency LED
Sensitivity Mode High-Sensitivity Detection
Software Functions Absolute Quantification, Relative Quantification, Melting Curve Analysis, High-Resolution Melting (HRM), Genotyping, Endpoint Fluorescence Analysis
Connectivity Ethernet, USB, Wi-Fi
Display 7-inch Full-Color Capacitive LCD Touchscreen
Dimensions 205 × 156 × 153 mm (L×W×H)
Weight 3.2 kg
Data Storage ≥1,000 runs onboard
Power Failure Recovery Yes — resumes interrupted runs upon reboot

Overview

The TIANLONG Gentier Mini and Mini+ are compact, field-deployable real-time fluorescent quantitative PCR systems engineered for precision nucleic acid amplification and detection under non-traditional laboratory conditions. Based on the principle of sequence-specific DNA amplification coupled with real-time fluorescence monitoring—using intercalating dyes (e.g., SYBR Green I, EvaGreen) or hydrolysis probes (e.g., FAM, HEX, ROX, Cy5)—these instruments deliver quantitative cycle (Cq)-based analysis with high thermal fidelity and optical reproducibility. Designed for mobile biosurveillance, point-of-care diagnostics, veterinary field testing, and decentralized clinical screening, the Gentier Mini series eliminates the need for dedicated HVAC-controlled lab spaces while maintaining compliance with core performance benchmarks expected in regulated molecular workflows.

Key Features

  • Ultra-portable architecture: Weighing only 3.2 kg and measuring under 21 cm in any dimension, the unit is certified for benchtop, vehicle-mounted, or hand-carried deployment without recalibration after relocation.
  • High-speed thermal cycling: Achieves maximum heating and cooling rates of 5.0 °C/s and 4.0 °C/s respectively, enabling rapid ramping across multi-step protocols—including touchdown PCR, long-amplicon amplification (>10 kb), and HRM profiling—without thermal overshoot or lag.
  • Four-channel optical detection: Independently optimized LED excitation and filter-matched photodiode detection support simultaneous acquisition across FAM/SYBR (Channel 1), HEX/VIC (Channel 2), Texas Red/ROX (Channel 3), and Cy5 (Channel 4), with full-spectrum data capture completed in ≤1 second per 16-well run.
  • Robust thermal uniformity: Patented Peltier-based block design ensures ≤±0.2 °C well-to-well temperature variance across the entire 16-well array, critical for reproducible Cq values and low inter-run CVs (<1.5% for standard curves).
  • Intelligent power resilience: Embedded uninterruptible operation logic retains protocol state during transient power loss; system automatically resumes from last completed cycle upon restoration—no manual reinitialization required.
  • Integrated touchscreen interface: 7-inch capacitive LCD enables fully standalone operation, including assay setup, real-time monitoring, result interpretation, and PDF report generation without external computing devices.

Sample Compatibility & Compliance

The Gentier Mini+ accepts standard 0.2 mL transparent single tubes and 8-tube strips, compatible with common qPCR chemistries including TaqMan probes, molecular beacons, scorpions, and saturation dyes. Its thermal block geometry and optical path are validated per ISO 20395:2019 (Biotechnology – Requirements for evaluating qPCR methods) and align with minimum performance criteria outlined in CLSI MM19-A3 and USP . While not pre-certified for IVD use in EU or FDA markets, the system supports GLP-compliant documentation through audit-trail-enabled software logs (user actions, timestamps, parameter changes) and encrypted data export—facilitating internal validation per GMP Annex 11 or 21 CFR Part 11 when deployed in quality-controlled environments.

Software & Data Management

The Gentier Control & Analysis Suite (v4.x) provides dual-mode operation: embedded firmware for offline execution and Windows/macOS desktop application for advanced visualization and batch processing. Core analytical modules include absolute quantification (standard curve and comparative Cq), relative quantification (ΔΔCq), endpoint fluorescence genotyping, melting curve derivation (with derivative peak analysis), and high-resolution melt (HRM) clustering. All raw fluorescence trajectories, thermal profiles, and metadata are stored in vendor-neutral .csv and .xlsx formats. Audit trails record user login/logout events, assay modifications, and result exports—supporting traceability requirements in regulated QC/QA labs. Data synchronization occurs via encrypted Wi-Fi, Ethernet, or direct USB transfer; no cloud dependency is required.

Applications

  • Veterinary disease surveillance: Rapid detection of ASFV, CSFV, PEDV, and avian influenza A (H5/H7/H9) in farm-side or border inspection settings.
  • Food safety testing: Screening for Salmonella spp., Listeria monocytogenes, and Cronobacter sakazakii in raw ingredients and finished products.
  • Plant pathogen diagnostics: Identification of phytoplasmas, viroids, and fungal pathogens (e.g., Fusarium oxysporum) in nursery stock and greenhouse samples.
  • Environmental monitoring: Quantification of fecal indicator bacteria (Enterococcus, E. coli) and antimicrobial resistance genes (e.g., blaCTX-M, vanA) in wastewater and surface water.
  • Academic and teaching labs: Low-cost platform for introducing students to qPCR fundamentals, primer optimization, and assay validation protocols.

FAQ

Does the Gentier Mini require routine optical calibration after transportation?
No. The instrument features a factory-calibrated, drift-compensated optical path with mechanical lock-in alignment—eliminating post-move recalibration per manufacturer specifications.
Can the system perform high-resolution melting (HRM) analysis?
Yes. Both Gentier Mini and Mini+ support continuous fluorescence acquisition during gradual ramping (0.02–0.2 °C/s), enabling discrimination of SNPs, methylation variants, and heteroduplex formation with sub-degree thermal resolution.
Is the software compliant with 21 CFR Part 11 for electronic records?
The desktop software offers optional configuration for electronic signatures, audit trail logging, and role-based access control—meeting foundational technical controls required for Part 11 adherence when implemented within an organization’s validated IT infrastructure.
What consumables are validated for use with this instrument?
Only 0.2 mL thin-wall transparent PCR tubes and 8-tube strips from certified suppliers (e.g., Axygen, Thermo Fisher, Bio-Rad) are recommended; opaque or frosted tubes may impair signal transmission and are not supported.
How is data integrity maintained during extended field deployments?
Onboard flash memory retains ≥1,000 complete run datasets with timestamped metadata; all exported files include digital checksums, and the firmware enforces write-protection on critical system partitions to prevent accidental corruption.

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