Cervical cancer rapid diagnostic test Aptima®
HPVHCVHBV

cervical cancer rapid diagnostic test
cervical cancer rapid diagnostic test
cervical cancer rapid diagnostic test
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Characteristics

Applications
for cervical cancer
Micro-organism
HPV, HCV, HBV

Description

The Aptima Virology portfolio delivers on the Hologic promise of innovation through life-changing viral testing for viruses that impact patients across the globe. Deliver Precise Results The industry-leading accuracy of Aptima assays for HIV-1, HCV and HBV give you the confidence to deliver reliable, repeatable results that you and your patients can count on. Experience Optimal Performance Aptima Virology assays operate on the Panther® system, which means ultra-fast, true sample-to-result automation—everything your lab needs to meet today’s molecular testing demands. Applied Innovation in Virology Testing Hologic and the Aptima Virology portfolio have a legacy of innovation and leadership, driving critical advances in the diagnosis and monitoring of Human Immunodeficiency Virus (HIV) and Hepatitis B and C viruses (HBV and HCV). This legacy began with the FDA approval of qualitative nucleic acid amplification tests (NAATs) for HIV-1 and HCV in the early 2000s. It continues with viral load testing for HIV-1, HCV, and HBV. Today, the Aptima Virology portfolio is a critical aid in the clinical management of HIV-1, HCV, and HBV. Run on the fully automated Panther system, these assays use proprietary real-time transcription mediated amplification (TMA) technology from Hologic.

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*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.