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tbs atm atr phosphosubstrate rabbit cell signaling  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc tbs atm atr phosphosubstrate rabbit cell signaling
    Tbs Atm Atr Phosphosubstrate Rabbit Cell Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tbs atm atr phosphosubstrate rabbit cell signaling/product/Cell Signaling Technology Inc
    Average 94 stars, based on 44 article reviews
    tbs atm atr phosphosubstrate rabbit cell signaling - by Bioz Stars, 2026-02
    94/100 stars

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    The scatterplot of biomarkers in IHC and ICC. (A) Scatterplot for AKT endometrial expression. (B) Scatterplot for mTOR endometrial expression. (C) Scatterplot for Pax-2 endometrial expression. IHC, immunohistochemistry; ICC, immunocytochemistry.

    Journal: Frontiers in Medicine

    Article Title: Immunocytochemical examination of Akt, mTOR, and Pax-2 for endometrial carcinoma through thin-layer endometrial cytology

    doi: 10.3389/fmed.2025.1576060

    Figure Lengend Snippet: The scatterplot of biomarkers in IHC and ICC. (A) Scatterplot for AKT endometrial expression. (B) Scatterplot for mTOR endometrial expression. (C) Scatterplot for Pax-2 endometrial expression. IHC, immunohistochemistry; ICC, immunocytochemistry.

    Article Snippet: The subsequent assays were conducted within a humidity-controlled environment as follows: (1) sections were incubated with EDTA at 60°C for 10 min; (2) sections were rinsed with PBS three times; (3) sections underwent overnight incubation with rabbit anti-human AKT antibody (#9611, Cell Signaling TechnologyTM, USA, 1:600 dilution), rabbit anti-human mTOR-related protein antibody (#2983, Cell Signaling TechnologyTM, USA, 1:150 dilution), and rabbit anti-human Pax-2 antibody (ZSGB-BIOTM, Beijing, China); (4) sections were rinsed four times with PBS (2 min per rinse); (5) ChemMateTM EnVisionTM/HRP (DakoTM, Herndon, VA, USA) was introduced, followed by incubation of the sections for 30 min at 37°C; (6) sections were rinsed four times with PBS; (7) staining was performed using 3,3-diaminobenzidine (DAB) at room temperature in the dark for 180 s; (8) distilled water halted the DAB staining; (9) sections were hematoxylin-stained; and (10) sections were dehydrated, cleared, and mounted with neutral-gum, with positive controls treated in the same manner.

    Techniques: Expressing, Immunohistochemistry, Immunocytochemistry

    ROC curve of biomarkers in IHC and ICC. (A) ROC curve for AKT. (B) ROC curve for mTOR. (C) ROC curve for Pax-2. The green line indicates ICC, and the blue line represents IHC. IHC, immunohistochemistry; ICC, immunocytochemistry.

    Journal: Frontiers in Medicine

    Article Title: Immunocytochemical examination of Akt, mTOR, and Pax-2 for endometrial carcinoma through thin-layer endometrial cytology

    doi: 10.3389/fmed.2025.1576060

    Figure Lengend Snippet: ROC curve of biomarkers in IHC and ICC. (A) ROC curve for AKT. (B) ROC curve for mTOR. (C) ROC curve for Pax-2. The green line indicates ICC, and the blue line represents IHC. IHC, immunohistochemistry; ICC, immunocytochemistry.

    Article Snippet: The subsequent assays were conducted within a humidity-controlled environment as follows: (1) sections were incubated with EDTA at 60°C for 10 min; (2) sections were rinsed with PBS three times; (3) sections underwent overnight incubation with rabbit anti-human AKT antibody (#9611, Cell Signaling TechnologyTM, USA, 1:600 dilution), rabbit anti-human mTOR-related protein antibody (#2983, Cell Signaling TechnologyTM, USA, 1:150 dilution), and rabbit anti-human Pax-2 antibody (ZSGB-BIOTM, Beijing, China); (4) sections were rinsed four times with PBS (2 min per rinse); (5) ChemMateTM EnVisionTM/HRP (DakoTM, Herndon, VA, USA) was introduced, followed by incubation of the sections for 30 min at 37°C; (6) sections were rinsed four times with PBS; (7) staining was performed using 3,3-diaminobenzidine (DAB) at room temperature in the dark for 180 s; (8) distilled water halted the DAB staining; (9) sections were hematoxylin-stained; and (10) sections were dehydrated, cleared, and mounted with neutral-gum, with positive controls treated in the same manner.

    Techniques: Immunohistochemistry, Immunocytochemistry