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Bioer GenePure Plus NPA-32+ Fully Automated Magnetic Bead-Based Nucleic Acid Extraction System

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Brand Bioer
Origin Zhejiang, China
Manufacturer Type Authorized Distributor
Instrument Type Magnetic Bead-Based Extraction System
Automation Level Dedicated Fully Automatic Platform
Sample Throughput per Run 1–32 samples
Sample Volume Range 20–1000 µL
Processing Time per Batch 15–45 minutes
Compatible Consumables 2.2 mL 96-well Deep-Well Plates
Interface RS232
Operating System Microsoft Windows 7 / 8.1 / 10
Dimensions (L×W×H) 440 × 380 × 450 mm
Net Weight 20 kg
Power Supply AC 100–240 V, 50/60 Hz, 450 W

Overview

The Bioer GenePure Plus NPA-32+ is a dedicated fully automated nucleic acid extraction system engineered for precision, reproducibility, and workflow efficiency in clinical diagnostics and molecular biology laboratories. It operates on the principle of magnetic bead-based solid-phase extraction—leveraging paramagnetic particles functionalized with silica or carboxyl groups that selectively bind nucleic acids under controlled chaotropic salt and pH conditions. During processing, the instrument precisely coordinates magnetic separation, liquid handling, temperature-controlled incubation (lysis, binding, washing, elution), and UV decontamination to isolate high-purity DNA or RNA from diverse biological matrices—including whole blood, buffy coat, saliva, cultured cells, tissue homogenates, and FFPE-derived lysates. Its integrated architecture eliminates manual pipetting steps while maintaining strict adherence to standardized extraction kinetics, ensuring consistent yield, integrity, and downstream compatibility with qPCR, NGS library preparation, Sanger sequencing, and digital PCR.

Key Features

  • Integrated 10.1-inch industrial-grade touchscreen tablet with intuitive graphical user interface for protocol selection, real-time run monitoring, and parameter adjustment
  • Dual-zone thermal control system: independent heating modules for lysis (up to 85 °C) and elution (up to 75 °C), with ±0.5 °C temperature uniformity across all wells
  • UV-C germicidal lamp (254 nm) mounted inside the processing chamber, activated automatically before and after each run to minimize cross-contamination risk
  • Positive-pressure air displacement pipetting with disposable plastic extraction tips and sealed 2.2 mL deep-well plates—eliminating carryover between samples and batches
  • Precision magnetic rod array with synchronized vertical/horizontal motion ensures uniform bead capture and efficient wash/elution cycles across all 32 positions
  • Preloaded library of validated extraction protocols optimized for common sample types and commercial reagent kits (e.g., QIAGEN, Takara, Thermo Fisher, and Bioer’s own MagPure series)

Sample Compatibility & Compliance

The GenePure Plus NPA-32+ supports extraction from human and non-human biological specimens compliant with ISO 20387:2018 (Biobanking), CLSI MM18-A (Molecular Diagnostic Methods), and CAP/CLIA pre-analytical requirements. It accommodates input volumes ranging from 20 µL (e.g., dried blood spots or micro-volume plasma) to 1000 µL (e.g., whole blood or cell suspensions), enabling flexibility across diagnostic screening, research cohort studies, and biobank operations. All consumables—including tip racks, deep-well plates, and magnetic bead reagents—are traceable via lot-number logging within the instrument’s audit trail. The system meets IEC 61000-4 electromagnetic compatibility standards and is designed for use in ISO Class 7 (10,000) cleanroom environments or certified biosafety cabinets when handling infectious samples.

Software & Data Management

The embedded Windows-based control software provides full GLP-compliant data governance: each run generates a timestamped electronic record containing operator ID, protocol version, start/stop times, temperature logs, magnetic actuation cycles, and error flags. Audit trails are immutable and exportable in CSV or PDF format for regulatory review. Software supports user role-based access control (administrator, technician, viewer), electronic signature capability per FDA 21 CFR Part 11 Annex A guidance, and optional integration with LIMS via RS232 serial communication using HL7-compatible ASCII command sets. Custom protocol development is enabled through a visual scripting module supporting conditional logic (e.g., “if volume > 500 µL, extend binding time by 2 min”) and multi-step thermal ramping profiles.

Applications

  • Clinical molecular testing: extraction of cfDNA from plasma for oncology liquid biopsy assays
  • High-throughput pathogen detection: parallel isolation of viral RNA (e.g., SARS-CoV-2, Influenza A/B) from nasopharyngeal swabs
  • Genetic screening workflows: automated gDNA purification from EDTA blood prior to SNP genotyping or exome sequencing
  • Single-cell and low-input applications: optimized protocols for ≤100 cells or ≤50 ng starting material with carrier RNA co-isolation
  • Quality control in biomanufacturing: routine nucleic acid recovery assessment from upstream bioreactor harvests or purified plasmid preps

FAQ

What types of magnetic bead kits are compatible with the GenePure Plus NPA-32+?
The system is validated for use with all major commercially available magnetic bead-based nucleic acid extraction kits requiring 2.2 mL deep-well plate formats—including Bioer MagPure, QIAGEN QIAamp, Thermo Fisher KingFisher Flex-compatible chemistries, and custom in-house formulations.
Does the instrument support remote monitoring or network connectivity?
While the NPA-32+ does not include built-in Ethernet or Wi-Fi, it supports RS232-to-Ethernet bridge configurations for centralized lab monitoring via third-party middleware; local USB export of run logs and reports is standard.
How is cross-contamination prevented between runs?
Contamination mitigation is achieved through three redundant layers: (1) disposable plastic tips and sealed deep-well plates, (2) internal UV-C irradiation (≥30 mJ/cm² dose) applied pre- and post-run, and (3) automated air-gap aspiration and tip ejection routines that prevent aerosol generation during liquid transfer.
Can the system be validated for GMP-regulated environments?
Yes—the platform supports IQ/OQ documentation packages, including temperature mapping reports, magnetic field uniformity verification, pipetting accuracy/precision testing (per ISO 8655), and software validation templates aligned with Annex 11 and USP analytical instrument qualification guidelines.

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