เม.ย. . 24, 2026 14:05 กลับไปยังรายการ
Human Papillomavirus (HPV) infection is the primary cause of cervical cancer, with certain high-risk genotypes responsible for the majority of cases worldwide. Among them, HPV 16, HPV 18, and HPV 45 are recognized as the most clinically significant types due to their strong association with high-grade lesions and invasive cervical cancer. Early and accurate detection of these high-risk HPV types is essential for timely intervention, risk assessment, and effective patient management.
การ Cowingene HPV 16/18/45 Detection Kit (NATBox) is an advanced in vitro diagnostic (IVD) solution designed for the qualitative detection of HPV DNA using real-time PCR technology. Integrated with the fully automated NATBox system, this kit provides a rapid, accurate, and streamlined molecular diagnostic solution for targeted cervical cancer screening.

This detection kit is intended for the qualitative detection of HPV DNA in clinical specimens, specifically identifying the following high-risk genotypes:
HPV 16
HPV 18
HPV 45
By focusing on these key oncogenic types, the kit provides clinicians with highly relevant diagnostic information for evaluating cervical cancer risk and determining appropriate follow-up strategies.
The test results serve as important auxiliary evidence for clinical diagnosis, screening, and monitoring of HPV-related infections, supporting early intervention and improved patient outcomes.
The kit supports the following specimen types:
Urine samples
Cervical swabs
This flexibility enables both non-invasive and clinician-collected sampling methods, improving patient compliance and facilitating broader participation in screening programs. Urine-based testing is especially valuable for large-scale or community-based screening initiatives.
A key highlight of this product is its integration with the NATBox® Mini II system, an automated molecular diagnostic platform that simplifies and standardizes the entire testing process.
The NATBox system performs:
Sample preparation
Nucleic acid extraction
PCR amplification
Target detection
within a single platform, significantly reducing manual intervention.
Each test uses a single-use cartridge that contains all necessary PCR reagents. This design offers:
Minimal risk of cross-contamination
Improved biosafety
Consistent and reproducible results
The compact and automated design makes the system suitable for:
Hospitals
Clinics
Decentralized laboratories
Resource-limited settings

The kit achieves a limit of detection (LoD) of 100 copies/mL for HPV 16, 18, and 45, enabling reliable detection even in low viral load samples and early-stage infections.
Validation studies confirm that the kit shows no cross-reactivity with non-target pathogens, including:
Chlamydia trachomatis
Neisseria gonorrhoeae
Candida albicans
Trichomonas vaginalis
Gardnerella vaginalis
Ureaplasma species and other HPV types
This ensures high diagnostic accuracy and reduces false-positive results.
The test performance is not affected by common interfering substances such as:
Hemoglobin
White blood cells
Cervical mucus
Vaginal care products and lubricants
Antibiotics such as metronidazole
This robustness ensures reliable performance under real clinical conditions.
The kit demonstrates excellent precision, with CV ≤ 10%, ensuring consistent results across:
Different testing days
Different reagent batches
Different operators and testing environments
Detection Method: Real-time PCR (automated NATBox system)
Detection Targets: HPV 16, 18, 45
Compatible Instrument: NATBox® มินิ II
Sample Types: ปัสสาวะ, สำลีเช็ดปากมดลูก
Storage Conditions: 2–8°C
Shelf Life: 12 months
Certification: CE-IVD
These specifications ensure high compatibility, reliability, and ease of use in clinical environments.
The kit can be used with a complete set of supporting reagents to optimize performance:
Sample collection kits (urine and vaginal)
Sample diluent reagents
NATBox system platform
This enables a standardized, closed, and efficient molecular diagnostic workflow, reducing hands-on time and improving laboratory throughput.
Targeted detection of HPV 16, 18, and 45, the most clinically significant genotypes
Fully automated NATBox system for simplified operation
High sensitivity (LoD 100 copies/mL) for early detection
Self-contained cartridge design to minimize contamination risk
Flexible sample types, including non-invasive urine samples
Strong specificity and anti-interference performance
Reduced turnaround time, enabling rapid clinical decisions
CE-IVD certified, ensuring quality and compliance
The Cowingene HPV 16/18/45 Detection Kit (NATBox) represents a significant advancement in molecular diagnostics by combining targeted high-risk HPV detection with fully automated PCR technology. Its integration with the NATBox system enables rapid, accurate, and user-friendly testing, making it ideal for both centralized laboratories and point-of-care settings.
By focusing on the most oncogenic HPV types and delivering high-performance results with minimal operational complexity, this kit supports early detection, improves clinical decision-making, and enhances cervical cancer prevention strategies.
As demand for efficient and scalable diagnostic solutions continues to grow, the NATBox-based HPV detection system offers a powerful tool for modern healthcare environments and global screening programs.
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