Genplex® Hpv PCR Genotype Detection Nucleic Acid Analysis System

Customization: Available
Classification: Physiological Functions of Diagnosis and Monitoring Equipment
Type: Molecular Diagnostic Instrument

Product Description

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Basic Information

  • Model NO.BHF-VI
  • CertificationCE, ISO13485
  • GroupFull Range
  • HS Code9027509090
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Technology Overview

The instrument utilizes reverse hybridization for qualitative virus sub-type analysis. Specimens are processed through an automated system that adds reagents, extracts DNA, and amplifies PCR via micro-pumps. Amplified products are then transferred to the test area for reverse hybridization. Target gene products are captured by specific probes, displaying visible spots after coloration to identify the virus sub-type. Negative specimens remain clear of spots.

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Specification

Nucleic Acid Chip Analyzer

The system comprises a host unit and an optional printer. The host unit is a sophisticated integration of multiple sub-systems:

  • 1. Image display system
  • 2. Automated Reagent Dispensing System
  • 3. Pneumatic Control System (positive/negative pressure)
  • 4. Temperature Control System
  • 5. Image Detection System
  • 6. 3D Movable Platform System

Sample Type: Exfoliated cervical epithelial cells

Application: Optimized for nucleic acid detection and analysis, specifically clinical screenings like HPV testing.

Nucleic Acid Analysis System Host Unit
Detection Module Detail 1
Detection Module Detail 2
Detection Module Detail 3
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Technical Specifications

Feature Details
ModelBHF-VI
Detection PlatformPCR & Reverse dot blot hybridization
Detection Modules6 Modules
Sample Capacity24
Heating Rate≥1.5 ℃/s (50℃ to 90℃)
Cooling Rate≥1.5 ℃/s (90℃ to 50℃)
Electrical Specification230V, 50Hz, 600VA
Dimension1000 x 610 x 690±10 (mm)
Weight≤80kg
Technical Specifications Chart
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Product Features

Simple
Only 5 minutes of hands-on time required.
Easy
No precise measuring or pipetting required for operation.
Fast
Complete turnaround time of approximately 3.5 hours.
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Comprehensive
Supports 24/28 target genotypes for Human Papillomavirus.
Feature Comparison
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Enterprise Profile

Corporate Banner

Founded in 2001, our group is a high-tech biomedical enterprise integrating R&D, production, sales, and after-sales service. We operate a massive 40,000 m² R&D center dedicated to medical innovation. We excel in molecular diagnosis, immunoassay, atomic absorption, and mass spectrometry.

Research Facility 1
Research Facility 2

Why Choose Our Solutions?

Our in-vitro diagnosis systems are used in over 4,000 hospitals, handling up to 22 million tests annually. Our automated nucleic acid testing leverages microfluidic "lab on a chip" technology, providing efficient service to diverse medical institutions worldwide.

Innovation Focus

Post-acquisition of leading spectrometry brands, our focus has expanded to life science mass spectrometry, delivering superior user experiences and cutting-edge products for molecular analysis.

Frequently Asked Questions

Q: Can I obtain samples of the reagents? A: Yes, samples are available for evaluation purposes.
Q: Is OEM or ODM service supported for custom logos? A: No, we currently do not support OEM/ODM services for these specific diagnostic products.
Q: Are you a professional manufacturer? A: Absolutely. We operate a professional manufacturing facility in the capital region and welcome professional visits.
Q: What is the monthly production capacity for the BHF-VI? A: Our facility produces approximately 2,000 units and 1 million person-time reagents per month.
Q: How soon will the goods be shipped after an order? A: Products are typically in stock and will be shipped within 7 business days.
Q: What specific clinical screenings is this system ideal for? A: The GenPlex® BHF-VI is highly optimized for nucleic acid detection and analysis, making it an ideal choice for HPV (Human Papillomavirus) testing.

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