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HPV RNA, Low and High Risk, ISH
Test Code37730
CPT Codes
88364, 88365
Preferred Specimen
Formalin-fixed, paraffin-embedded tissue in IHC specimen transport kit
Other Acceptable Specimens
11 unstained charged (+) slides submitted in IHC specimen transport kit
Instructions
Do not place labels with adhesive backing on slides. Use pencil or xylene-resistant pen to write on the frosted end of the slide only.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: Indefinitely
Refrigerated: Indefinitely
Frozen: Unacceptable
Refrigerated: Indefinitely
Frozen: Unacceptable
Methodology
In-Situ Hybridization (ISH)
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set Up: Mon-Sat; Report Available: 2-5 days
Clinical Significance
HPV is the causative agent of cervical dysplasia and carcinoma. Selected low-risk and high-risk subtypes are assessed in tissue block.