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Introduction
Product Features
Specification
Q&A
24 HUMAN PAPILLOMAVIRUS TYPING KIT (Liquid&Lyophilized)
Genotypes Identification
This kit is intended to qualitatively detect the deoxyribonucleic acid (DNA) of 24 types of human papillomavirus (HPV) in women's cervical shedding cell samples, and identify HPV as 16, 18 ,31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 26, 53, 66, 73, 82, 6, 11, 42, 43, 44 or 81 genotypes. It is used for assisted diagnosis of HPV infection.
Introduction
Product Features
Specification
Q&A
Introduction

Why do we test HPV? 


Cervical cancer is a leading cause of mortality among women. In 2020, an estimated 604 000 women were diagnosed with cervical cancer worldwide and about 342 000 women died from the disease. In the new WHO guideline for screening and treatment of cervical pre-cancer lesions for cervical cancer prevention, WHO suggests among the general population of women at the age of 30 years screening HPV every 5 to 10 years. 


WHO suggests using an HPV DNA primary screening test either with triage or without triage to prevent cervical cancer among the general population of women. 


Introduction More
Product Features
Specification
Product Name
24 HUMAN PAPILLOMAVIRUS TYPING KIT (Liquid&Lyophilized)
Package Specification
24 Tests/Kit | 48 Tests/Box
Storage Condition

The shelf life of this kit is 12 months when stored at – (20±5) oC. It is suggested to transport the kits in a sealed foam box with ice packs. Never leave the kit for more than 7 days at 2-8 oC under light avoidance.

Performance

Coincidence of references

By using National reference panel for the complete genome of Human Papillomavirus genotyping to evaluate this kit, the results were consistent with both positive references and negative references. For enterprise references, the coincidence rates of 11 negative references and 24 positive references are both 100%.

The limit of detection (LoD)

The limit of detection for all targeted HPV types are 500 copies/mL-1.

Precision

The coefficient of variation of Ct values of precision references is not higher than 5% within-batch and inter-batch.

Interfering substances

10% white blood cells, 5% lubricant, 2% antibacterial lotion, 2mg/mL-1 hemoglobin, 0.1mg/mL-1 of mucin,10mg/mL-1 benzene ether embolism or 4mg/mL-1 nitric acid contained in the sample had no significant influence on the performance of the kit. However, still try to avoid any interference substances in the process of sampling.


Q & A
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