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antiproliferating cell nuclear antigen (pcna) pc10  (Agilent technologies)


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    Structured Review

    Agilent technologies antiproliferating cell nuclear antigen (pcna) pc10
    Antiproliferating Cell Nuclear Antigen (Pcna) Pc10, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cell+nuclear+antigen+(pcna%3B+pc10/pm38844257-55-2-11
    Average 90 stars, based on 1 article reviews
    antiproliferating cell nuclear antigen (pcna) pc10 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Incubation:

    Article Title: Bioerodible wraps and uses therefor
    Article Snippet: .. Following this, the samples were incubated with a primary mouse monoclonal antibody against human PCNA (Dako Cytomation, Clone PC10, Denmark) overnight at 4° C. in a moist chamber to prevent sample drying. ..

    Immunostaining:

    Article Title: Nail growth arrest under low body temperature during hibernation
    Article Snippet: .. Immunostaining was performed using antibodies against phosphor-Histone H3 (pH3) (06-570, Merck), PCNA (PC10, DAKO), anti-Ki67 antibody (ab16667, Abcam). ..

    other:

    Article Title: Preclinical development of non-viral gene therapy for patients with advanced pancreatic cancer
    Article Snippet: Slides were next incubated overnight at 4°C with anti-PCNA (DakoCytomation, clone PC10, ref M0879, dilution: 1:100), or SSTR2 antibodies (AbCAM clone [UMB1] ref ab134152, dilution: 1:100) diluted in Antibody diluent (DakoCytomation).

    Article Title: Triple negative breast cancer cells exposed to aryl hydrocarbon receptor ligands hexachlorobenzene and chlorpyrifos activate endothelial cells.
    Article Snippet: Breast cancer is currently one of the most prevalent cancers worldwide.. The mechanisms by which pesticides can increase breast cancer risk are multiple and complex.. We have previously observed that two aryl hydrocarbon receptor (AhR) agonists ‒pesticides hexachlorobenzene (HCB) and chlorpyrifos (CPF)‒ act on tumor progression, stimulating cell migration and invasion in vitro and tumor growth in animal models.

    Article Title: Differential effect of asparagine and glutamine removal on three adenocarcinoma cell lines
    Article Snippet: Thereafter, samples were washed in PBS, fixed in 4 % formaldehyde for 5 min and permeabilized in 70 % ethanol at −20 °C for 20 min. After blocking, samples were incubated with the primary PC10 anti-PCNA antibody (1:100 dilution, Dako, RRID: M0879) for 1 h and, then, with the secondary anti-mouse Alexa 488 antibody (dilution 1:200, Invitrogen, RRID: AB_141708 ) for 30 min. Alternatively, cells were incubated with the primary anti-RPA70 antibody (1:100 dilution, Cell Signaling Technologies, RRID: AB_2180506 ) and then with the secondary anti-rabbit Dylight 594 antibody (1:200 dilution, Abcam, RRID: AB_10680407 ).

    Article Title: Omics and imaging combinatorial approach reveals butyrate-induced inflammatory effects in the zebrafish gut
    Article Snippet: Samples were stained using an automated staining machine (Autostainer Link 48, Dako Agilent, CA, USA) with anti-proliferating cell nuclear antigen (PCNA mouse mAb Clone PC10, M0879, Dako A/S, Denmark, diluted 1:10.000) or with anti-Zeta chain of T cell receptor associated protein kinase 70 (ZAP70 Rabbit mAb 99F2, Cell Signaling Technology USA, diluted 1:300) antibodies to study proliferating cells (epithelial renewal) as well as NK-like cells and T cells.

    Article Title: Breast cancer progression and kynurenine pathway enzymes are induced by hexachlorobenzene exposure in a Her2-positive model.
    Article Snippet: Breast cancer is one of the leading cancers among women worldwide.. Given the evidence that pesticides play an important role in breast cancer, interest has grown in pesticide impact on disease progression.. Hexachlorobenzene (HCB), an aryl hydrocarbon receptor (AhR) ligand, promotes triple-negative breast cancer cell migration and invasion.



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    Image Search Results


    VAD and further refeeding with a VAS diet cause changes in cell proliferation in the mammary gland. (A) Immunohistochemistry for PCNA in the mammary gland. The black arrows indicate positive PCNA + cells. Magnification 100×. The scale bar represents 25 μm. (B) Quantification of the percentage of PCNA + cells from the immunohistochemistry images shown in (A). Data are shown as representative images or mean values ± SDs ( n = 10).

    Journal: Oxidative Medicine and Cellular Longevity

    Article Title: Apoptosis in the Mammary Gland of Virgin Rats Subchronically Fed With a Vitamin A Deficient Diet

    doi: 10.1155/omcl/6334165

    Figure Lengend Snippet: VAD and further refeeding with a VAS diet cause changes in cell proliferation in the mammary gland. (A) Immunohistochemistry for PCNA in the mammary gland. The black arrows indicate positive PCNA + cells. Magnification 100×. The scale bar represents 25 μm. (B) Quantification of the percentage of PCNA + cells from the immunohistochemistry images shown in (A). Data are shown as representative images or mean values ± SDs ( n = 10).

    Article Snippet: The sections were incubated with the following primary antibodies: 8 h in a humidified chamber at 4°C with mouse monoclonal antihuman BCL-2 (clon BCL-2/100; Catalog. No. AM287-5M, BioGenex, San Ramón, CA, USA), 30 min in a humidified chamber at 20°C with rabbit polyclonal antihuman BAX protein (Catalog. No. AR347-5R, BioGenex, San Ramón, CA, USA), and for 4 h in a humidified chamber at 20°C with mouse monoclonal anti-rat proliferating cell nuclear antigen (PCNA) (clon PC10; Catalog. No. AM252-5M, BioGenex, San Ramón, CA, USA).

    Techniques: Immunohistochemistry

    VAS and further refeeding with a VAS diet cause changes in apoptosis and proliferation in the mammary gland. Determination of the TUNEL + /PCNA + cell ratios from the immunohistochemistry images shown in Figures A and A. The data are presented as the means ± SDs ( n = 4).

    Journal: Oxidative Medicine and Cellular Longevity

    Article Title: Apoptosis in the Mammary Gland of Virgin Rats Subchronically Fed With a Vitamin A Deficient Diet

    doi: 10.1155/omcl/6334165

    Figure Lengend Snippet: VAS and further refeeding with a VAS diet cause changes in apoptosis and proliferation in the mammary gland. Determination of the TUNEL + /PCNA + cell ratios from the immunohistochemistry images shown in Figures A and A. The data are presented as the means ± SDs ( n = 4).

    Article Snippet: The sections were incubated with the following primary antibodies: 8 h in a humidified chamber at 4°C with mouse monoclonal antihuman BCL-2 (clon BCL-2/100; Catalog. No. AM287-5M, BioGenex, San Ramón, CA, USA), 30 min in a humidified chamber at 20°C with rabbit polyclonal antihuman BAX protein (Catalog. No. AR347-5R, BioGenex, San Ramón, CA, USA), and for 4 h in a humidified chamber at 20°C with mouse monoclonal anti-rat proliferating cell nuclear antigen (PCNA) (clon PC10; Catalog. No. AM252-5M, BioGenex, San Ramón, CA, USA).

    Techniques: TUNEL Assay, Immunohistochemistry

    Effect of YM on PCNA ( A ) and Caspase-3 H ( B ) in lenses. Data are expressed as the means ± SD, a p < 0.05 vs. C, b p < 0.05 vs. HC. C: control group, HC: hydrocortisone group, YM: yerba mate aqueous extract, YM-1: YM 62.5 mg/kg group, YM-2: YM 125 mg/kg group, YM-3: YM 250 mg/kg group.

    Journal: Life

    Article Title: Anti-Cataract Effect of the Traditional Aqueous Extract of Yerba Mate ( Ilex paraguariensis A. St.-Hil.): An In Ovo Perspective

    doi: 10.3390/life14080994

    Figure Lengend Snippet: Effect of YM on PCNA ( A ) and Caspase-3 H ( B ) in lenses. Data are expressed as the means ± SD, a p < 0.05 vs. C, b p < 0.05 vs. HC. C: control group, HC: hydrocortisone group, YM: yerba mate aqueous extract, YM-1: YM 62.5 mg/kg group, YM-2: YM 125 mg/kg group, YM-3: YM 250 mg/kg group.

    Article Snippet: The prepared samples were stained with antiproliferative cell nuclear antigen (PCNA) (Novus, NB500-106, Littleton, CO, USA) to assess proliferation and caspase-3 (Novus-NB100-56708) to assess apoptosis (antibodies are compatible with chick).

    Techniques: Control

    Caspase-3 ( a ) and PCNA ( b ) staining in lenses. I: C, II: HC, III: YM-1, IV: YM-2, V: YM-3. C: control group, HC: hydrocortisone group, YM: yerba mate aqueous extract, YM-1: YM 62.5 mg/kg group, YM-2: YM 125 mg/kg group, YM-3: YM 250 mg/kg group.

    Journal: Life

    Article Title: Anti-Cataract Effect of the Traditional Aqueous Extract of Yerba Mate ( Ilex paraguariensis A. St.-Hil.): An In Ovo Perspective

    doi: 10.3390/life14080994

    Figure Lengend Snippet: Caspase-3 ( a ) and PCNA ( b ) staining in lenses. I: C, II: HC, III: YM-1, IV: YM-2, V: YM-3. C: control group, HC: hydrocortisone group, YM: yerba mate aqueous extract, YM-1: YM 62.5 mg/kg group, YM-2: YM 125 mg/kg group, YM-3: YM 250 mg/kg group.

    Article Snippet: The prepared samples were stained with antiproliferative cell nuclear antigen (PCNA) (Novus, NB500-106, Littleton, CO, USA) to assess proliferation and caspase-3 (Novus-NB100-56708) to assess apoptosis (antibodies are compatible with chick).

    Techniques: Staining, Control