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Nucleic Acid Detection and HPV 16/18 Genotyping Kit for 14 Types of High-Risk Human Papillomavirus (Fluorescent PCR)
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Nucleic Acid Detection and HPV 16/18 Genotyping Kit for 14 Types of High-Risk Human Papillomavirus (Fluorescent PCR)

HPV-DNA is a mandatory screening test for cervical cancer in women regulated by the FDA.
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Product description

HPV-DNA is a mandatory screening test for cervical cancer in women regulated by the FDA.


Cervical cancer is currently the only cancer with a clear cause. HPV infection with the high-risk HPV is found in 97% of cervical cancer patients. 


High-risk types of HPV -- especially HPV16 and HPV18 -- cause genital warts, external genital cancer, cervical cancer and high cervical intraepithelial neoplasia. 

 

 

HPV High Risk Detection:
HPV16,18,31,33,35,39,45,51,52,56,58,59,68,66
HPV Genotyping:
HPV 16, HPV 18
Sample type:
Female cervical exfoliated cell

 

Application
● Direct detection of HPV-DNA
● More sensitive, specific, accurate and rapid
● Estimate viral load and cancer risk
● Evaluate HPV vaccine efficacy and prognosis efficacy

 

* Comparision between Kindmay FAM fluorescence detection channel and reference reagent

 

Test site
12 high-risk HPV-FAM fluorescence channel detection
Reference reagent
Total
+
-
Hospital 1
Kindmay High-Risk HPVnucleic acid detection kit
+
124
1
125
-
9
77
86
Hospital 2
Kindmay High-Risk HPVnucleic acid detection kit
+
146
5
151
-
11
158
169
Hospital 3
Kindmay High-Risk HPVnucleic acid detection kit
+
87
2
89
-
8
140
148
Total 
385
383
768

 

 

Compared with the reference reagent, Kindmay High-Risk HPV nucleic acid detection kit:

 

The positive coincidence rate: 92.7%.

 

The negative coincidence rate: 97.9%.

 

The overall coincidence rate: 95.3%.

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