PreTect See | Quality control test for NILM cytology
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PreTect SEE

PreTect SEE

PreTect SEE is ideal as a quality control test for NILM cytology. It is an assay for the qualitative detection of the presence of Human Papillomavirus, HPV, E6/E7 oncogene mRNA from carcinogenic HPV types 16, 18 and 45.

 

PreTect SEE shows high clinical specificity, supported by a low positive rate in the general population.

 

This CE-IVD kit identify women that have carcinogenic expression of high-risk HPV types that may induce cervical cancer. Co-testing with PreTect SEE and Cytology will therefore improve the existing screening program sensitivity without an excessive follow-up workload.

 

With its high capacity and low cost the test is also ideal as stand-alone test in low-income countries.

Clinical benefits 

Qualitative detection of E6/E7 mRNA expression from HPV 16, 18, 45

Intrinsic sample control ensuring sample adequacy

High clinical specificity minimising unnecessary interventions

High PPV for CIN2+

Enhanches identification of cervical adenocarcinoma

Low positivity rate in general population

CE-IVD kit

Test information

  
Individual HPV genotyping E6/E7 mRNA HPV 16, 18 and 45
Intrinsic Sample Control (ISC):Targeting mRNA from housekeeping gene
Sample type:Cervical samples
Preservatives:PreTect TM (PreTect AS)
PreservCyt/ThinPrep (Hologic)
SurePath (BD Diagnostics)
Input-material:Isolated Nucleic Acid (DNA/RNA)*
Technology:Real time NASBA
Isothermal amplification (41°C)
Four specific molecular beacons
Format:96-well PCR plate
Pre-filled with reagents
n=94
Assay time:~ 150 minutes
Instrumentation:Fluorescence reader /
RT-PCR (CFX-96/QuantStudio5)
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