TEST DIRECTORY

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Laboratory:Akiruno

Lung cancer PD-L1 protein (IHC)22C3

  • TEST NAME SPECIMEN SUBMISSION SPECIMEN
    REQUIREMENT
    CONTAINER CAP COLOR STORE
    TEMPERATURE
    (STABILITY)
    TURNAROUND
    TIME (DAY)
    METHODOLOGY
  • Lung cancer PD-L1 protein (IHC)22C3
    Unstained specimen slide 4 pieces Z10 Room temperature
    5-7 Immunohistochemical staining method

COMMENT


How to Submit Lung Carcinoma PD-L1 Protein (IHC) 22C3
1) Since the presence or absence of carcinoma cells may be unknown, please attach a copy of the pathology report when requesting the test. (However, this is not required if the company is conducing general pathology tests.) If for some reason you cannot attach this information, please include the name of the pathology diagnosis (tissue type, etc.) and as much clinical information, etc. as possible in the request form.
2) Materials shall be unstained specimen slides (prepared from formalin-fixed paraffin blocks) of lung carcinoma (primary or metastatic). Please use silane or other coating slides, and after thinly sectioning, dry the slides overnight at approximately 40°C before submission.
3) Thinly section the tissue to a thickness of 4-5 μm and attach on the center to the extent possible, at least 15 mm away from the frosted glass edge and 15 mm away from the glass slide edge.
4) When requesting with paraffin blocks, please contact with our sales staff as the turnaround time will be delayed due to the preparation of unstained specimen slides.

Please use silane or other coating slides, and after thinly sectioning, dry the slides overnight at approximately 40°C before submission.
3) Thinly section the tissue to a thickness of 4-5 μm and attach on the center to the extent possible, at least 15 mm away from the frosted glass edge and 15 mm away from the glass slide edge.

CONTAINER

supplementary information



肺癌 PD-L1タンパク (IHC) 22C3 の注意事項

  • 判定基準
    TPS(%) 判定
    0 陰性
    1-49 発現あり
    50以上 高発現
    TPS (Tumor Proportion Score): 腫瘍細胞中のPD-L1発現陽性細胞の割合
  • ペムブロリズマブの投与基準
    (試薬添付文書より)
    対象患者 投与基準
    既治療 非小細胞肺癌 TPSが1%以上
    未治療 非小細胞肺癌 TPSが50%以上

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