Cervical cancer test kit S014T048B0C2
for sexually transmitted diseasesfor genotypingfor genes

cervical cancer test kit
cervical cancer test kit
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Characteristics

Applications
for cervical cancer, for sexually transmitted diseases, for genotyping
Tested parameter
for genes
Micro-organism
HPV
Sample type
for cervical cells
Analysis mode
for PCR

Description

24 genotyping HPV Test Kit 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. 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. 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%.
*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.