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rabbit anti mouse ki67 monoclonal antibody  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti mouse ki67 monoclonal antibody
    Rabbit Anti Mouse Ki67 Monoclonal Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1281 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+ki+67/Ki-67+Rabbit+mAb/pm41881227-328-37-42
    Average 97 stars, based on 1281 article reviews
    rabbit anti mouse ki67 monoclonal antibody - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    other:

    Article Title: Limited in-depth invasion of Fusobacterium nucleatum into in vitro reconstructed human gingiva.
    Article Snippet: The primary antibodies (Abs) and titrations used were: mouse monoclonal Ki-67, clone MIB-1 (DAKO A/S, Golstrup, Denmark), 1:25; rabbit monoclonal cleaved caspase-3 (Cell signalling Technology Inc., Beverly, MA, USA), 1:250; mouse monoclonal MMP-13 (1:30) and mouse monoclonal E-cadherin (1:9000) (R&D Systems Inc., Minneapolis, MN, USA).

    Article Title: Destabilized Adhesion in the Gastric Proliferative Zone and c-Src Kinase Activation Mark the Development of Early Diffuse Gastric Cancer
    Article Snippet: The following primary antibodies were used: rabbit polyclonal E-cadherin (sc7870, dilution 1:100), mouse monoclonal c-Src (sc8056, 1:1,000), rabbit polyclonal Fak (sc932, 1:1,000), all from Santa Cruz Biotechnology (Santa Cruz, CA); sheep polyclonal pepsinogen II (ab9013, 1:1,000), rabbit polyclonal Lin-7 (ab11472, 1:500), and mouse monoclonal h-actin (ab6276, 1:3,000) were from Abcam (Cambridge, United Kingdom); rabbit polyclonal fibronectin (A0245, 1:2000), mouse monoclonal Ki-67 (M7240, 1:50), and mouse monoclonal cytokeratin AE1/AE3 (A0245, 1:50) were from DAKO (Glostrup, Denmark); mouse monoclonal Stat3 (9139, 1:200) and mouse monoclonal pY705-Stat3 (9138, 1:60) were from Cell Signaling; mouse monoclonal Dnmt1 (IMG-261, 1:250; Imgenex, San Diego, CA), rabbit polyclonal pY861-Fak (44-626, 1:250; Biosource), mouse monoclonal H+/K+ATPase h subunit (RDI-HKATPabm, 1:500; Research Diagnostics), mouse monoclonal p120 (610133, 1:3,000; BD Transduction Labs, San Jose, CA), mouse monoclonal MUC5A and MUC6 (NCLMUC-5AC, NCL-MUC-6, both 1:50; Novocastra, Newcastle Upon Tyne, United Kingdom), and mouse monoclonal activated c-Src (clone 28, 1:250, from ACube, and a kind gift from Dr. Koji Owada, Kyoto Pharmaceutical University, Japan).



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    Representative cross-sections of the neonatal myocardium on postnatal day 14 (P14), following a 48-h hyperoxia (HY) exposure period (P5–P7) and a recovery phase labeled with nuclear-localized proliferation marker <t>Ki67</t> (red) and DAPI (blue), shown with normoxia (NO, 21% O 2 , upper left), with verum groups hyperoxia (HY, 80% O 2 , lower left), hyperoxia with CBD 10 mg/kg (HY10, upper right), and hyperoxia with CBD 30 mg/kg (HY30, lower right). The outlined regions (white bordered boxes) are magnified 4.3× compared to the original image. All cardiac cross-sections were obtained at the midventricular level and are presented in a standardized orientation. LV, left ventricle; RV, right ventricle; 100× magnification.
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    Representative cross-sections of the neonatal myocardium on postnatal day 14 (P14), following a 48-h hyperoxia (HY) exposure period (P5–P7) and a recovery phase labeled with nuclear-localized proliferation marker <t>Ki67</t> (red) and DAPI (blue), shown with normoxia (NO, 21% O 2 , upper left), with verum groups hyperoxia (HY, 80% O 2 , lower left), hyperoxia with CBD 10 mg/kg (HY10, upper right), and hyperoxia with CBD 30 mg/kg (HY30, lower right). The outlined regions (white bordered boxes) are magnified 4.3× compared to the original image. All cardiac cross-sections were obtained at the midventricular level and are presented in a standardized orientation. LV, left ventricle; RV, right ventricle; 100× magnification.
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    Image Search Results


    Graphical Representation of Survival Probabilities of QDB - related Indicators and Diagnostic Performance of NIPI (a) The threshold value of MTP53 by QDB was 0.16 nmol/g. (b) The threshold value of Ki-67 by QDB was 11.9 nmol/g. (c) NIPI-QDB had statistical significance. (d) The AUC of NIPI-QDB was 0.8. NIPI: Novel international prognostic index, QDB: Quantitative dot blot, AUC: Area under curve.

    Journal: CytoJournal

    Article Title: Development and validation of a multiparameter prognostic model for extranodal natural killer/T-cell lymphoma: Integration of clinical, pathological, and molecular biomarkers

    doi: 10.25259/Cytojournal_34_2025

    Figure Lengend Snippet: Graphical Representation of Survival Probabilities of QDB - related Indicators and Diagnostic Performance of NIPI (a) The threshold value of MTP53 by QDB was 0.16 nmol/g. (b) The threshold value of Ki-67 by QDB was 11.9 nmol/g. (c) NIPI-QDB had statistical significance. (d) The AUC of NIPI-QDB was 0.8. NIPI: Novel international prognostic index, QDB: Quantitative dot blot, AUC: Area under curve.

    Article Snippet: 2 , Ki-67 (clone number: MIB-1; 20220920) , Beijing Zhongshan Jinqiao Biotechnology Co., Ltd..

    Techniques: Diagnostic Assay, Quantitative Dot Blot

    Representative cross-sections of the neonatal myocardium on postnatal day 14 (P14), following a 48-h hyperoxia (HY) exposure period (P5–P7) and a recovery phase labeled with nuclear-localized proliferation marker Ki67 (red) and DAPI (blue), shown with normoxia (NO, 21% O 2 , upper left), with verum groups hyperoxia (HY, 80% O 2 , lower left), hyperoxia with CBD 10 mg/kg (HY10, upper right), and hyperoxia with CBD 30 mg/kg (HY30, lower right). The outlined regions (white bordered boxes) are magnified 4.3× compared to the original image. All cardiac cross-sections were obtained at the midventricular level and are presented in a standardized orientation. LV, left ventricle; RV, right ventricle; 100× magnification.

    Journal: International Journal of Molecular Sciences

    Article Title: Cannabidiol Protects the Neonatal Mouse Heart from Hyperoxia-Induced Injury

    doi: 10.3390/ijms27010146

    Figure Lengend Snippet: Representative cross-sections of the neonatal myocardium on postnatal day 14 (P14), following a 48-h hyperoxia (HY) exposure period (P5–P7) and a recovery phase labeled with nuclear-localized proliferation marker Ki67 (red) and DAPI (blue), shown with normoxia (NO, 21% O 2 , upper left), with verum groups hyperoxia (HY, 80% O 2 , lower left), hyperoxia with CBD 10 mg/kg (HY10, upper right), and hyperoxia with CBD 30 mg/kg (HY30, lower right). The outlined regions (white bordered boxes) are magnified 4.3× compared to the original image. All cardiac cross-sections were obtained at the midventricular level and are presented in a standardized orientation. LV, left ventricle; RV, right ventricle; 100× magnification.

    Article Snippet: The sections were incubated overnight at 4 °C with the primary antibody, monoclonal rabbit anti-mouse Ki67 (1:250, Cell Signal Technology, Danvers, MA, USA, Cat. 9129S), diluted in antibody diluent (Zymed Laboratories, San Francisco, CA, USA, Cat. ZUC103).

    Techniques: Labeling, Marker

    Quantification of ( A ) Ki67 immunostaining and cell cycling transcripts for ( B ) CycD1 , ( C ) CycD2 , and ( D ) Gas2l3 of whole hearts for P7 after 2 days of oxygen exposure and recovery until P14 using qPCR. Data are normalized to the level of mouse pups exposed to normoxia at each time point (control 100%, NO, 21% O 2 , white bars) with verum groups hyperoxia (HY, 80% O 2 , black), hyperoxia with CBD 10 mg/kg (HY10, light grey), and hyperoxia with CBD 30 mg/kg (HY30, dark grey). Data are presented as box–whisker plots, with n = 12 per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001 (ANOVA; Brown–Forsythe).

    Journal: International Journal of Molecular Sciences

    Article Title: Cannabidiol Protects the Neonatal Mouse Heart from Hyperoxia-Induced Injury

    doi: 10.3390/ijms27010146

    Figure Lengend Snippet: Quantification of ( A ) Ki67 immunostaining and cell cycling transcripts for ( B ) CycD1 , ( C ) CycD2 , and ( D ) Gas2l3 of whole hearts for P7 after 2 days of oxygen exposure and recovery until P14 using qPCR. Data are normalized to the level of mouse pups exposed to normoxia at each time point (control 100%, NO, 21% O 2 , white bars) with verum groups hyperoxia (HY, 80% O 2 , black), hyperoxia with CBD 10 mg/kg (HY10, light grey), and hyperoxia with CBD 30 mg/kg (HY30, dark grey). Data are presented as box–whisker plots, with n = 12 per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001 (ANOVA; Brown–Forsythe).

    Article Snippet: The sections were incubated overnight at 4 °C with the primary antibody, monoclonal rabbit anti-mouse Ki67 (1:250, Cell Signal Technology, Danvers, MA, USA, Cat. 9129S), diluted in antibody diluent (Zymed Laboratories, San Francisco, CA, USA, Cat. ZUC103).

    Techniques: Immunostaining, Control, Whisker Assay