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cell nuclear staining solution dapi  (Beyotime)


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    Structured Review

    Beyotime cell nuclear staining solution dapi
    Cell Nuclear Staining Solution Dapi, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 33033 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dapi+staining+solution+c1002/DAPI/pm40849365-49-0-8
    Average 99 stars, based on 33033 article reviews
    cell nuclear staining solution dapi - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Incubation:

    Article Title: Zyxin protects against hypertensive nephropathy by restraining FAK/Skp2-CDK8/YAP signaling in tubular epithelial cells.
    Article Snippet: 1 Department of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China 2 Department of Nephrology, Huadong Hospital, Fudan University, Yan’an Road No. 221, Shanghai 200040, China Abstract Background Tubulointerstitial fibrosis and inflammation are hallmark pathological features of hypertensive nephropathy (HN), yet the underlying molecular mechanisms remain elusive.. Zyxin, a focal adhesion protein, has been implicated in hypertension-related pathologies, but its specific role in HN-induced tubulointerstitial injury remains undefined.. Methods An HN murine model was established via a multi-hit DOCA/Ang II + uninephrectomy + high salt approach.

    Article Title: SERINC3 promotes oral squamous cell carcinoma progression and mitochondrial metabolic reprogramming involving c-MET/JNK/PGC-1α axis.
    Article Snippet: .. Cells were incubated with the working solution (100 nM) at 37°C for 20 min and fixed with 4% paraformaldehyde for 20 min. Then cells were washed again with PBS and treated with a fluorescence quenching agent containing DAPI (Beyotime, P0131, China) to protect the fluorescent signal. ..

    Staining:

    Article Title: Zyxin protects against hypertensive nephropathy by restraining FAK/Skp2-CDK8/YAP signaling in tubular epithelial cells.
    Article Snippet: 1 Department of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China 2 Department of Nephrology, Huadong Hospital, Fudan University, Yan’an Road No. 221, Shanghai 200040, China Abstract Background Tubulointerstitial fibrosis and inflammation are hallmark pathological features of hypertensive nephropathy (HN), yet the underlying molecular mechanisms remain elusive.. Zyxin, a focal adhesion protein, has been implicated in hypertension-related pathologies, but its specific role in HN-induced tubulointerstitial injury remains undefined.. Methods An HN murine model was established via a multi-hit DOCA/Ang II + uninephrectomy + high salt approach.

    Article Title: Sex-Stratified Characterization of Behavioral, Hippocampal, and Microglial Androgen Responses to Adolescent High-Fat Diet Consumption in Mice.
    Article Snippet: .. Finally, the cell nuclei were stained with 4,6-diamidino-2-phenylindole (DAPI; C1027, 1:600; Beyotime, Shanghai, China). ..

    Article Title: Targeting MMGT1 enhances immunotherapy efficacy in triple-negative breast cancer.
    Article Snippet: The following day, Alexa Fluor 488-labeled goat anti-mouse IgG (Abcam, ab150113) or Alexa Fluor 594-labeled goat anti-rabbit IgG (Abcam, ab150080) was added and incubated for 1 h in the dark. .. Finally, nuclei were stained with DAPI (Beyotime, C1006) for 5 min, and images were captured using a confocal fluorescence microscope (Leica, Germany). ..

    Article Title: Platelet-derived microparticles induce CD8 + T cell senescence in chronic kidney disease via the transfer of microRNA-550a-5p.
    Article Snippet: .. Nuclei were stained with DAPI (Beyotime). .. Visualization was performed using a Zeiss LSM800 NLO confocal microscopy (Carl Zeiss).

    Glass:

    Article Title: HOXA3 Knockdown Impairs hESC-Derived Thymic Epithelial-like Cell Differentiation and CXCL12-Associated Early T-Lineage Support.
    Article Snippet: .. Nuclei were counterstained with DAPI (Beyotime, Biotechnology, Shanghai, China) for 10 min at room temperature in the dark, and coverslips were mounted onto glass slides using an anti-fade mounting medium (Beyotime, China). .. Images were acquired using a Zeiss 880 multiphoton laser scanning microscope (Zeiss, Oberkochen, Germany) or a Nikon single-photon confocal microscope (Nikon, Tokyo, Japan).

    Fluorescence:

    Article Title: SERINC3 promotes oral squamous cell carcinoma progression and mitochondrial metabolic reprogramming involving c-MET/JNK/PGC-1α axis.
    Article Snippet: .. Cells were incubated with the working solution (100 nM) at 37°C for 20 min and fixed with 4% paraformaldehyde for 20 min. Then cells were washed again with PBS and treated with a fluorescence quenching agent containing DAPI (Beyotime, P0131, China) to protect the fluorescent signal. ..

    Article Title: Targeting MMGT1 enhances immunotherapy efficacy in triple-negative breast cancer.
    Article Snippet: The following day, Alexa Fluor 488-labeled goat anti-mouse IgG (Abcam, ab150113) or Alexa Fluor 594-labeled goat anti-rabbit IgG (Abcam, ab150080) was added and incubated for 1 h in the dark. .. Finally, nuclei were stained with DAPI (Beyotime, C1006) for 5 min, and images were captured using a confocal fluorescence microscope (Leica, Germany). ..

    Confocal:

    Article Title: Targeting MMGT1 enhances immunotherapy efficacy in triple-negative breast cancer.
    Article Snippet: The following day, Alexa Fluor 488-labeled goat anti-mouse IgG (Abcam, ab150113) or Alexa Fluor 594-labeled goat anti-rabbit IgG (Abcam, ab150080) was added and incubated for 1 h in the dark. .. Finally, nuclei were stained with DAPI (Beyotime, C1006) for 5 min, and images were captured using a confocal fluorescence microscope (Leica, Germany). ..

    Microscopy:

    Article Title: Targeting MMGT1 enhances immunotherapy efficacy in triple-negative breast cancer.
    Article Snippet: The following day, Alexa Fluor 488-labeled goat anti-mouse IgG (Abcam, ab150113) or Alexa Fluor 594-labeled goat anti-rabbit IgG (Abcam, ab150080) was added and incubated for 1 h in the dark. .. Finally, nuclei were stained with DAPI (Beyotime, C1006) for 5 min, and images were captured using a confocal fluorescence microscope (Leica, Germany). ..

    Modification:

    Article Title: Multimodal Programming of Extracellular Vesicles via Nano-Primed SECCS-Based 3D Microenvironments for Coordinated Ferroptosis Suppression and Myogenic Regeneration in Diabetes.
    Article Snippet: Chronic diabetic glucolipotoxicity is associated with progressive skeletal muscle atrophy, bone loss, cellular senescence, and ferroptotic injury.. Because ferroptosis inhibition alonemay not restore compromisedmyogenic capacity, we developed a combined stem cell-conditioning strategy integrating fullerol priming with the stem cell screen-enrich-combine(-biomaterials) circulating system (SECCS).. This integrated three-dimensional culture platform uses porous β-TCP granules and intermittent medium circulation to generate BMSCs-derived extracellular vesicles (EVs).

    Saline:

    Article Title: Multimodal Programming of Extracellular Vesicles via Nano-Primed SECCS-Based 3D Microenvironments for Coordinated Ferroptosis Suppression and Myogenic Regeneration in Diabetes.
    Article Snippet: Chronic diabetic glucolipotoxicity is associated with progressive skeletal muscle atrophy, bone loss, cellular senescence, and ferroptotic injury.. Because ferroptosis inhibition alonemay not restore compromisedmyogenic capacity, we developed a combined stem cell-conditioning strategy integrating fullerol priming with the stem cell screen-enrich-combine(-biomaterials) circulating system (SECCS).. This integrated three-dimensional culture platform uses porous β-TCP granules and intermittent medium circulation to generate BMSCs-derived extracellular vesicles (EVs).



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    Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence <t>(DAPI)</t> represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.
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    Beyotime cell nuclear staining solution dapi
    Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence <t>(DAPI)</t> represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.
    Cell Nuclear Staining Solution Dapi, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dapi+staining+solution+c1002/DAPI/pm40849365-49-0-8
    Average 99 stars, based on 1 article reviews
    cell nuclear staining solution dapi - by Bioz Stars, 2026-10
    99/100 stars
      Buy from Supplier

    Image Search Results


    Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence (DAPI) represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.

    Journal: Journal of Advanced Research

    Article Title: Increased Rab1a accelerates osteoarthritis by inhibiting autophagy via activation of the mTORC1-S6K pathway

    doi: 10.1016/j.jare.2024.11.009

    Figure Lengend Snippet: Rab1a exaggerated extracellular matrix degradation and apoptosis in mice. A) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Rab1a AAV or control AAV were exhibited via immunohistochemical analysis, Scale bar, 20 μm. B) Protein deposition of Rab1a, MMP13, ADAMTS5, and Aggrecan in articular cartilage with transfection by Ad-Rab1a or Ad-NC were detected using immunohistochemical analysis, scale bar, 20 μm. C) Quantification of A. n = 6. D) Quantification of B. n = 6. E, F) TUNEL staining of chondrocytes in hyaline cartilage (HC) and calcified cartilage (CC) of each group. Blue fluorescence (DAPI) represented the nucleus, and green fluorescence (fluorescein-dUTP) represented TUNEL-positive cells. Scale bar, 25 μm. G, H) Quantification of TUNEL-positive chondrocytes relative to total chondrocytes was shown. n = 6. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. TUNEL: TdT-mediated dUTP Nick-End Labeling.

    Article Snippet: Subsequently, The TUNEL reaction mixture was applied at room temperature for 1 h. This was followed by coloring the nuclei with DAPI Staining Solution(Beyotime, China).

    Techniques: Transfection, Control, Immunohistochemical staining, TUNEL Assay, Staining, Fluorescence, End Labeling