| Type: | IVD Reagent |
|---|---|
| Spec: | 32 T/Kit |
| Transport Package: | Paper Carton with Icy Bag |
| Specification: | 44*44*45 cm |
| Trademark: | Tianlong |
| Origin: | Suzhou Shaanxi |
| Samples: |
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| Customization: |
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Audited Supplier Product Name:
Human Papilloma Virus (HPV) Nucleic Acid Detection Kit (Fluorescence PCR Method)
Intended Use:
The TianLong Human Papilloma Virus(HPV) Nucleic Acid Detection Kit is a qualititative in vitro test for detection of 18 high-risk HPV types(HPV 16,18,26,31,33,35,39,45,51,52,53,56,58,59,66,68,73 and 82) by Real-time Polymerase Chain Reaction (Real-time PCR) method.
This test is designed to detect HPV DNA in specimens such as female cervical epithelial cells.
The potential candidate personnel to be tested could include, but are not limited to patients with symptoms of infection who are suspected of HPV by healthcare providers, or persons with no symptoms from a population for screening test confirmation or exclusion of viral infection or viral carriage status.
Results from the test are for the identification of HPV existence in samples tested. The HPV are mostly often detectable in female cervical epithelial cells samples collected during the acute phase of infection.
| Product Name |
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| Cat.No | P120H | |
| Specification | 32T/Kit | |
| Specimen | Female cervical epithelial cells | |
| Storage & Validity | All reagents should be stored at -20ºC±5 ºC. The validity period of the reagents is 12 months. | |
| Applicable Equipment | Instruments with FAM ,HEX/VIC,CY5 and TEXAS RED/ROX channels, such as ABI7500 real time PCR systems, Gentier series real time PCR systems |
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Audited Supplier 
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