TEST DIRECTORY

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Laboratory：Akiruno

○HPV nucleic acid detection(Medical examination)

CODE：00W58 5

  • TEST NAME SPECIMEN
    REQUIREMENT
    （ｍL）     CONTAINER CAP COLOR STORE
    TEMPERATURE
    (STABILITY)     TURNAROUND
    TIME (DAY)     METHODOLOGY REFERENCE RANGE
    (UNIT)
  • HPV nucleic acid detection(Medical examination)
    Uterine cervix
    V41 Room temperature
    （28 days）
     2-4 PCR (Real Time PCR)

    Real-time PCR
    A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

     Negative (－)

COMMENT


Requests cannot be made for containers other than the designated container (V41).
Please note that if the sample is contaminated with blood, the data may be affected.
This testing method is more susceptible to contamination, so please be careful when handling samples.


*Notes
-This is a test item for cervical cancer screening using HPV testing alone.
-If the result of this test is ”positive (+)”, an additional ”gynecological cytology test (triage)” will be performed.
-The required number of days for ”gynecological cytology (triage)” is 4 to 7 days.
-We use Roche Diagnostics' ”Cobas ®6800/8800 System HPV.”
The targets for measurement are types 16，18，and other high-risk groups (types 31，33，35，39，45，51，52，56，58，59，68，and 66).
-Samples will not be returned.

CONTAINER

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