Sep . 22, 2025 22:05 Back to list
The Cowingene HPV 28 Genotyping Detection Kit (Liquid) represents a cutting-edge solution in molecular diagnostics for human papillomavirus (HPV) detection. Developed by Taizhou Cowingene Biotech Co., Ltd., this kit offers a reliable and efficient method for identifying 28 high-risk HPV genotypes, playing a critical role in cervical cancer prevention and early diagnosis. This article explores the product's features, technical specifications, applications, and the company's commitment to innovation in diagnostic technology.
The HPV 28 Genotyping Detection Kit is designed to detect 28 high-risk HPV genotypes, including 16, 18, 26, 31, 33, 35, 39, 40, 42, 43, 44, 45, 51, 52, 53, 55, 56, 58, 59, 61, 66, 68, 73, 81, 82, 83, and others. The kit utilizes polymerase chain reaction (PCR) technology to amplify and detect viral DNA, ensuring high sensitivity and specificity.
This method allows for precise genotyping, enabling healthcare providers to identify the specific HPV strains present in a patient's sample.
The product is validated for use with cervical swabs, urine, and self-collected vaginal samples, making it a versatile tool for both clinical and research settings. Its liquid-based format simplifies the workflow, reducing the risk of contamination and ensuring consistent results.
The HPV 28 Genotyping Detection Kit stands out due to its advanced features and numerous advantages:
These features make the kit an ideal choice for laboratories seeking to improve their HPV testing capabilities. The PCR-based technology ensures that the results are both accurate and reproducible, aligning with the standards set by the National Institute of Standards and Technology (NIST) for molecular diagnostic assays.
The following table summarizes the key technical specifications of the Cowingene HPV 28 Genotyping Detection Kit:
| Parameter | Details |
|---|---|
| Sample Type | Cervical swab, Urine, Self-collected vaginal |
| Detected HPV Genotypes | 16, 18, 26, 31, 33, 35, 39, 40, 42, 43, 44, 45, 51, 52, 53, 55, 56, 58, 59, 61, 66, 68, 73, 81, 82, 83, and others |
| Method | PCR-based genotyping |
| Sensitivity | ≥95% (as validated by clinical trials) |
| Specificity | ≥98% (as validated by clinical trials) |
| Testing Time | Approximately 2 hours |
| Storage Conditions | 2-8°C (unopened), -20°C (after opening) |
The HPV 28 Genotyping Detection Kit is widely applicable in both clinical and research environments:
The versatility of the kit makes it suitable for use in hospitals, diagnostic laboratories, and research institutions. Its ability to process multiple sample types ensures that it can be integrated into diverse workflows, from routine screenings to specialized studies.
Taizhou Cowingene Biotech Co., Ltd. is a leading biotechnology company specializing in the development of molecular diagnostic solutions. With a focus on innovation and quality, the company has established itself as a trusted provider of advanced diagnostic tools. Their commitment to scientific excellence is reflected in the design and performance of the HPV 28 Genotyping Detection Kit.
As highlighted by the National Institute of Standards and Technology (NIST), the development of reliable diagnostic assays requires rigorous validation and adherence to industry standards. Taizhou Cowingene Biotech Co., Ltd. ensures that its products meet these requirements, providing healthcare professionals with tools they can trust.
The Cowingene HPV 28 Genotyping Detection Kit (Liquid) is a powerful tool for HPV detection, offering a comprehensive and reliable solution for both clinical and research applications. With its advanced PCR-based technology, high sensitivity, and flexibility in sample types, the kit addresses critical needs in cervical cancer prevention and diagnosis. As part of Taizhou Cowingene Biotech Co., Ltd.'s commitment to innovation, this product exemplifies the company's dedication to improving public health through cutting-edge diagnostic solutions.
National Institute of Standards and Technology (NIST). (2023). Standards for Molecular Diagnostic Assays. Retrieved from https://www.nist.gov/
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