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Laboratory:Hachioji

Human papillomavirus DNA (type 16, type 18, and other high-risk groups)

  • TEST NAME SPECIMEN
    REQUIREMENT
    (mL)
    CONTAINER CAP COLOR STORE
    TEMPERATURE
    (STABILITY)
    TURNAROUND
    TIME (DAY)
    METHODOLOGY REFERENCE RANGE
    (UNIT)
  • Human papillomavirus DNA (type 16, type 18, and other high-risk groups)
    Uterine cervix
    3.0
    V41 Room temperature
    2-4 PCR (Real Time PCR)

    Real-time PCR
    It is a type of nucleic acid amplification methods based on PCR method as the basic principle, which is a measurement method that, by using oligonucleotides that emit fluorescence when degraded, enables quantitative of target nucleic acids in real time by confirming the fluorescence signals in each PCR cycle.

    HPV type 16 negative
    HPV type 18 negative
    Other high-risk groups negative

COMMENT


The measurement targets are 16 type, 18 type, and other high risk groups (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68 type, and 66 type). Regarding "Other High Risk Groups", it is not determined by type. Please note that if the sample contains blood, it may affect the data. With this testing method, the affects of contamination are greater, so please be careful when handling the specimen.
[6471 1] Human papillomavirus DNA (type 16, type 18, and other high risk groups), [6487 1] About human papillomavirus (HPV) genotype determination
[2326 0] Cytodiagnosis (gynecology LBC) Or [6241 8]Cytodiagnosis (Gynecology LBC Bethesda System) can only be requested at the same time, but in that case, the required time for cytodiagnosis will be delayed by 1-2 days.

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