Double-dyeing kit for cervical intraepithelial neoplasia grading assisted diagnosis, and applications thereof
A technology for auxiliary diagnosis and kits, applied in analytical materials, measuring devices, instruments, etc., can solve the problems of affecting treatment plan selection and prognosis, interfering with CIN grading, low specificity, etc., to increase readability and accuracy, The effect of accurate CIN classification and accurate information
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Embodiment 1
[0059] The research object was formalin-fixed-paraffin-embedded normal cervical epithelial tissue (provided by Guangzhou Da'an Clinical Laboratory Center Co., Ltd.), and the grading and identification steps were as follows:
[0060] 1) Dewaxing and hydration: Before dewaxing, place tissue slices on a 60°C oven for 2 hours, soak in xylene for 10 minutes x 2 times, soak in absolute ethanol for 5 minutes x 2 times, 95% ethanol Soak in water for 5 minutes, soak in distilled water for 1 minute;
[0061] 2) Antigen retrieval: slices were repaired by boiling in EDTA antigen retrieval solution with a pH of 9.0, cooled, rinsed with tap water, and soaked in distilled water;
[0062] 3) Sealing: incubate with 3% hydrogen peroxide at room temperature for 10 minutes, rinse with distilled water, wash with TBS and soak;
[0063] 4) Double staining: add Stathmin antibody and MCM2 antibody dropwise, the titers of both antibodies are 100; incubate at room temperature for 60 minutes, wash with ...
Embodiment 2
[0070] The research objects were formalin-fixed-paraffin-embedded CINI and CINII cervical lesion tissues (provided by Guangzhou Da'an Clinical Laboratory Center Co., Ltd.), and the grading and identification steps were as follows:
[0071] 1) Dewaxing and hydration: Before dewaxing, place tissue slices on a 60°C oven for 2 hours, soak in xylene for 10 minutes x 2 times, soak in absolute ethanol for 5 minutes x 2 times, 95% ethanol Soak in water for 5 minutes, soak in distilled water for 1 minute;
[0072] 2) Antigen retrieval: slices were repaired by boiling in EDTA antigen retrieval solution with pH 9.0, cooled, rinsed with tap water, and soaked in distilled water;
[0073] 3) Sealing: incubate with 3% hydrogen peroxide at room temperature for 10 minutes, rinse with distilled water, wash with TBS and soak;
[0074] 4) Double staining: add Stathmin antibody and MCM2 antibody dropwise, the titers of both antibodies are 100; incubate at room temperature for 60 minutes, wash wit...
Embodiment 3
[0081] The research object was formalin-fixed-paraffin-embedded CINIII cervical lesion tissue (provided by Guangzhou Da'an Clinical Laboratory Center Co., Ltd.), and the grading and identification steps were as follows:
[0082] 1) Dewaxing and hydration: Before dewaxing, place tissue sections on a 60°C oven for 2 hours, soak in xylene for 10 minutes x 2 times, soak in absolute ethanol for 5 minutes x 2 times, and soak in 95% ethanol Soak for 5 minutes, soak in distilled water for 1 minute;
[0083] 2) Antigen retrieval: slices were repaired by boiling in EDTA antigen retrieval solution with pH 9.0, cooled, rinsed with tap water, and soaked in distilled water;
[0084] 3) Sealing: incubate with 3% hydrogen peroxide at room temperature for 10 minutes, rinse with distilled water, wash with TBS and soak;
[0085] 4) Double staining: add Stathmin antibody and MCM2 antibody dropwise, the titers of both antibodies are 100; incubate at room temperature for 60 minutes, wash with TBS,...
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