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dapi staining solution  (Beyotime)


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    Structured Review

    Beyotime dapi staining solution
    Dapi Staining Solution, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 2029 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/staining+with+dapi/DAPI+Staining+Solution/pmc13097096-64-0-21
    Average 99 stars, based on 2029 article reviews
    dapi staining solution - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Staining:

    Article Title: α -Ketoglutarate protects against cartilage damage via epigenetically driven metabolic reprogramming in osteoarthritis models
    Article Snippet: Immunofluorescence staining was carried out by incubation overnight at 4°C with antibodies against COL1A1 (Servicebio, GB11022-1; 1:200), Aspn (Affinity, DF13642; 1:100), Cilp (Huabio, ER1906-32; 1:100), Clu (Proteintech, 66109-1-Ig; 1:100), and Cnmd (Affinity, DF13715; 1:100). .. Alexa Fluor 594– or Cy3-conjugated secondary antibodies (Invitrogen) were added for 30 minutes, followed by staining with DAPI (Beyotime). .. Images were acquired with CaseViewer 2.3 scanning software (Servicebio), and analyzed with ImageJ software (NIH; version 1.8.0_112).

    Article Title: Exploring the role of RPS2 in muscle-invasive bladder cancer progression and resistance: A nanovesicle-based therapeutic approach
    Article Snippet: Newly synthesized RNA was labeled using the Cell-Light EU RNA Imaging Kit (C10316; RiboBio, Guangzhou, China). .. Cells were incubated with EU for 3h, followed by nuclear staining with DAPI (C1002; Beyotime Biotechnology) for 5 min. Fluorescence images were acquired with a fluorescence microscope (FV-1000/ES; Olympus), and 6–10 random fields were analyzed per sample. ..

    Article Title: Autophagy-induced osteoblast-derived exosomes maintain bone formation and prevent osteoporosis by remodeling gut microbiota-metabolism
    Article Snippet: After blocking in 3 % BSA for half an hour, osteoblasts were incubated with a primary antibody anti -LC3 (1:500, 14600-1-AP, Proteintech, USA) at 4 °C overnight. .. Afterward, incubation with a secondary antibody Goat Anti-Rabbit Alexa Flour 488 (1:300, ab150077, Abcam, UK) was conducted at room temperature for 1 h. After staining with DAPI (C1006, Beyotime), the fluorescence was observed under a fluorescence microscope. ..

    Article Title: The HKDC1-ASS1-ACSBG2 axis reprograms lipid metabolism to drive therapeutic resistance in hepatocellular carcinoma
    Article Snippet: .. After three washes with PBST, the cells were incubated with fluorescent secondary antibodies (Beyotime, Shanghai, China) for 1 h, followed by nuclear staining with DAPI (Beyotime, Shanghai, China). ..

    Article Title: ROS-responsive Prussian blue nanoplatform for synergistic myocardial ischemia/reperfusion injury therapy via EGCG delivery and DJ-1 pathway regulation.
    Article Snippet: Effective management of myocardial ischemia/reperfusion (I/R) injury remains a clinical challenge.. Epigallocatechin gallate (EGCG), a natural antioxidant, exhibits therapeutic potential in I/R models; however, it is limited by poor bioavailability and inadequate targeted delivery.. Therefore, using a synergistic therapeutic strategy, we designed a nanoplatform (PB@PEI@FPBA-EGCG NPs, referred to as PPFE NPs) to address these limitations.

    Article Title: Dihydrolipoic acid suppresses ferroptosis in chondrocytes to ameliorate the progression of osteoarthritis by modulating the FOXO1/TXNIP signaling pathway.
    Article Snippet: .. On the second day, after 1 h of incubation with secondary antibodies in the dark at room temperature, the cells were then subjected to nuclear staining with DAPI (#C1002, Beyotime). .. A Leica confocal laser scanning microscope was used to acquire fluorescence images.

    Article Title: After Traumatic Brain Injury, EPHA4 Enhances Endoplasmic Reticulum Stress to Promote M1 Microglial Polarization Through the MAPK Signaling Pathway
    Article Snippet: After the cell culture was complete, the medium was discarded, and the cells were fixed with 4% paraformaldehyde for 20 min. Then, the cells were incubated with primary antibodies against iNOS (1:200; 22226‐1‐AP; Proteintech, China) and Arg1 (1:200; 16001‐1‐AP; Proteintech, China) at 4°C overnight. .. Afterward, the corresponding fluorescent secondary antibody was incubated at room temperature for 2 h. After nuclear staining with DAPI (C1002; Beyotime, China) for 15 min, the cells were observed, and images were captured under a fluorescence microscope. .. The mean fluorescence intensity was quantified using ImageJ software.

    Article Title: Combined strategy of dual-module cerium nanosystem composite extracellular vesicles regulate ROS in the tissue microenvironment to promote periodontitis recovery
    Article Snippet: .. Cells were incubated with Vari Fluor 594-Phalloidin or Vari Fluor 488-Phalloidin (MCE) in the dark for 20 min, followed by nuclear staining with DAPI (P0131, Beyotime Biotechnology, China) for 10 min. Observations were performed using a confocal laser scanning microscope (CLSM; Olympus FV3000, Japan). .. The reactive oxygen species (ROS) detection kit (Beyotime Biotechnology, China) was used to evaluate the oxidative stress level in Raw264.7 macrophages.

    Incubation:

    Article Title: Exploring the role of RPS2 in muscle-invasive bladder cancer progression and resistance: A nanovesicle-based therapeutic approach
    Article Snippet: Newly synthesized RNA was labeled using the Cell-Light EU RNA Imaging Kit (C10316; RiboBio, Guangzhou, China). .. Cells were incubated with EU for 3h, followed by nuclear staining with DAPI (C1002; Beyotime Biotechnology) for 5 min. Fluorescence images were acquired with a fluorescence microscope (FV-1000/ES; Olympus), and 6–10 random fields were analyzed per sample. ..

    Article Title: Autophagy-induced osteoblast-derived exosomes maintain bone formation and prevent osteoporosis by remodeling gut microbiota-metabolism
    Article Snippet: After blocking in 3 % BSA for half an hour, osteoblasts were incubated with a primary antibody anti -LC3 (1:500, 14600-1-AP, Proteintech, USA) at 4 °C overnight. .. Afterward, incubation with a secondary antibody Goat Anti-Rabbit Alexa Flour 488 (1:300, ab150077, Abcam, UK) was conducted at room temperature for 1 h. After staining with DAPI (C1006, Beyotime), the fluorescence was observed under a fluorescence microscope. ..

    Article Title: The HKDC1-ASS1-ACSBG2 axis reprograms lipid metabolism to drive therapeutic resistance in hepatocellular carcinoma
    Article Snippet: .. After three washes with PBST, the cells were incubated with fluorescent secondary antibodies (Beyotime, Shanghai, China) for 1 h, followed by nuclear staining with DAPI (Beyotime, Shanghai, China). ..

    Article Title: ROS-responsive Prussian blue nanoplatform for synergistic myocardial ischemia/reperfusion injury therapy via EGCG delivery and DJ-1 pathway regulation.
    Article Snippet: Effective management of myocardial ischemia/reperfusion (I/R) injury remains a clinical challenge.. Epigallocatechin gallate (EGCG), a natural antioxidant, exhibits therapeutic potential in I/R models; however, it is limited by poor bioavailability and inadequate targeted delivery.. Therefore, using a synergistic therapeutic strategy, we designed a nanoplatform (PB@PEI@FPBA-EGCG NPs, referred to as PPFE NPs) to address these limitations.

    Article Title: Dihydrolipoic acid suppresses ferroptosis in chondrocytes to ameliorate the progression of osteoarthritis by modulating the FOXO1/TXNIP signaling pathway.
    Article Snippet: .. On the second day, after 1 h of incubation with secondary antibodies in the dark at room temperature, the cells were then subjected to nuclear staining with DAPI (#C1002, Beyotime). .. A Leica confocal laser scanning microscope was used to acquire fluorescence images.

    Article Title: After Traumatic Brain Injury, EPHA4 Enhances Endoplasmic Reticulum Stress to Promote M1 Microglial Polarization Through the MAPK Signaling Pathway
    Article Snippet: After the cell culture was complete, the medium was discarded, and the cells were fixed with 4% paraformaldehyde for 20 min. Then, the cells were incubated with primary antibodies against iNOS (1:200; 22226‐1‐AP; Proteintech, China) and Arg1 (1:200; 16001‐1‐AP; Proteintech, China) at 4°C overnight. .. Afterward, the corresponding fluorescent secondary antibody was incubated at room temperature for 2 h. After nuclear staining with DAPI (C1002; Beyotime, China) for 15 min, the cells were observed, and images were captured under a fluorescence microscope. .. The mean fluorescence intensity was quantified using ImageJ software.

    Article Title: Combined strategy of dual-module cerium nanosystem composite extracellular vesicles regulate ROS in the tissue microenvironment to promote periodontitis recovery
    Article Snippet: .. Cells were incubated with Vari Fluor 594-Phalloidin or Vari Fluor 488-Phalloidin (MCE) in the dark for 20 min, followed by nuclear staining with DAPI (P0131, Beyotime Biotechnology, China) for 10 min. Observations were performed using a confocal laser scanning microscope (CLSM; Olympus FV3000, Japan). .. The reactive oxygen species (ROS) detection kit (Beyotime Biotechnology, China) was used to evaluate the oxidative stress level in Raw264.7 macrophages.

    Fluorescence:

    Article Title: Exploring the role of RPS2 in muscle-invasive bladder cancer progression and resistance: A nanovesicle-based therapeutic approach
    Article Snippet: Newly synthesized RNA was labeled using the Cell-Light EU RNA Imaging Kit (C10316; RiboBio, Guangzhou, China). .. Cells were incubated with EU for 3h, followed by nuclear staining with DAPI (C1002; Beyotime Biotechnology) for 5 min. Fluorescence images were acquired with a fluorescence microscope (FV-1000/ES; Olympus), and 6–10 random fields were analyzed per sample. ..

    Article Title: Autophagy-induced osteoblast-derived exosomes maintain bone formation and prevent osteoporosis by remodeling gut microbiota-metabolism
    Article Snippet: After blocking in 3 % BSA for half an hour, osteoblasts were incubated with a primary antibody anti -LC3 (1:500, 14600-1-AP, Proteintech, USA) at 4 °C overnight. .. Afterward, incubation with a secondary antibody Goat Anti-Rabbit Alexa Flour 488 (1:300, ab150077, Abcam, UK) was conducted at room temperature for 1 h. After staining with DAPI (C1006, Beyotime), the fluorescence was observed under a fluorescence microscope. ..

    Article Title: After Traumatic Brain Injury, EPHA4 Enhances Endoplasmic Reticulum Stress to Promote M1 Microglial Polarization Through the MAPK Signaling Pathway
    Article Snippet: After the cell culture was complete, the medium was discarded, and the cells were fixed with 4% paraformaldehyde for 20 min. Then, the cells were incubated with primary antibodies against iNOS (1:200; 22226‐1‐AP; Proteintech, China) and Arg1 (1:200; 16001‐1‐AP; Proteintech, China) at 4°C overnight. .. Afterward, the corresponding fluorescent secondary antibody was incubated at room temperature for 2 h. After nuclear staining with DAPI (C1002; Beyotime, China) for 15 min, the cells were observed, and images were captured under a fluorescence microscope. .. The mean fluorescence intensity was quantified using ImageJ software.

    Microscopy:

    Article Title: Exploring the role of RPS2 in muscle-invasive bladder cancer progression and resistance: A nanovesicle-based therapeutic approach
    Article Snippet: Newly synthesized RNA was labeled using the Cell-Light EU RNA Imaging Kit (C10316; RiboBio, Guangzhou, China). .. Cells were incubated with EU for 3h, followed by nuclear staining with DAPI (C1002; Beyotime Biotechnology) for 5 min. Fluorescence images were acquired with a fluorescence microscope (FV-1000/ES; Olympus), and 6–10 random fields were analyzed per sample. ..

    Article Title: Autophagy-induced osteoblast-derived exosomes maintain bone formation and prevent osteoporosis by remodeling gut microbiota-metabolism
    Article Snippet: After blocking in 3 % BSA for half an hour, osteoblasts were incubated with a primary antibody anti -LC3 (1:500, 14600-1-AP, Proteintech, USA) at 4 °C overnight. .. Afterward, incubation with a secondary antibody Goat Anti-Rabbit Alexa Flour 488 (1:300, ab150077, Abcam, UK) was conducted at room temperature for 1 h. After staining with DAPI (C1006, Beyotime), the fluorescence was observed under a fluorescence microscope. ..

    Article Title: After Traumatic Brain Injury, EPHA4 Enhances Endoplasmic Reticulum Stress to Promote M1 Microglial Polarization Through the MAPK Signaling Pathway
    Article Snippet: After the cell culture was complete, the medium was discarded, and the cells were fixed with 4% paraformaldehyde for 20 min. Then, the cells were incubated with primary antibodies against iNOS (1:200; 22226‐1‐AP; Proteintech, China) and Arg1 (1:200; 16001‐1‐AP; Proteintech, China) at 4°C overnight. .. Afterward, the corresponding fluorescent secondary antibody was incubated at room temperature for 2 h. After nuclear staining with DAPI (C1002; Beyotime, China) for 15 min, the cells were observed, and images were captured under a fluorescence microscope. .. The mean fluorescence intensity was quantified using ImageJ software.

    Laser-Scanning Microscopy:

    Article Title: Combined strategy of dual-module cerium nanosystem composite extracellular vesicles regulate ROS in the tissue microenvironment to promote periodontitis recovery
    Article Snippet: .. Cells were incubated with Vari Fluor 594-Phalloidin or Vari Fluor 488-Phalloidin (MCE) in the dark for 20 min, followed by nuclear staining with DAPI (P0131, Beyotime Biotechnology, China) for 10 min. Observations were performed using a confocal laser scanning microscope (CLSM; Olympus FV3000, Japan). .. The reactive oxygen species (ROS) detection kit (Beyotime Biotechnology, China) was used to evaluate the oxidative stress level in Raw264.7 macrophages.

    Confocal Laser Scanning Microscopy:

    Article Title: Combined strategy of dual-module cerium nanosystem composite extracellular vesicles regulate ROS in the tissue microenvironment to promote periodontitis recovery
    Article Snippet: .. Cells were incubated with Vari Fluor 594-Phalloidin or Vari Fluor 488-Phalloidin (MCE) in the dark for 20 min, followed by nuclear staining with DAPI (P0131, Beyotime Biotechnology, China) for 10 min. Observations were performed using a confocal laser scanning microscope (CLSM; Olympus FV3000, Japan). .. The reactive oxygen species (ROS) detection kit (Beyotime Biotechnology, China) was used to evaluate the oxidative stress level in Raw264.7 macrophages.



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    Image Search Results


    Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. Phalloidin/DAPI staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.

    Journal: Biomaterials and Biosystems

    Article Title: The influence of simulated microgravity on MG-63 osteoblast-like cells cultured on polymeric scaffold

    doi: 10.1016/j.bbiosy.2026.100137

    Figure Lengend Snippet: Live/dead staining results in Experiment 1 (A, C, E, G) and Experiment 2 (B, D, F, H) of MG-63 cells cultured on (A, B) Glass, (C, D) Sc _plate, (E, F) Sc _v_static, (G, H) Sc _v_RPM. Living cells stained green by calcein-AM, dead cells stained red by propidium iodide. Phalloidin/DAPI staining results in Experiment 2: (B2) Glass, (D2) Sc _plate, (F2) Sc _v_static, (H2) Sc _v_RPM. Actin filaments stained green by phalloidin, cell nuclei stained blue by DAPI. Glass – cells seeded on glass coverslips and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _plate – cells seeded on scaffolds in the well plates and cultured in standard conditions (37 °C, 5 % CO 2 ), Sc _v_static – cells seeded on scaffolds, enclosed in the vials (37 °C), Sc _v_RPM – cells seeded on scaffolds, enclosed in the vials (37 °C), and subjected to the 60 rpm (Experiment 1) and 10 rpm (Experiment 2) settings on the RPM. Scale bar =100 µm.

    Article Snippet: Cell culture evaluation was performed using AlamarBlue Cell Viability test (ThermoFisher), lactate dehydrogenase activity assay (LDH, Takara, Saint-Germain-en-Laye, France), ALP activity assay based on p-nitrophenol (Sigma Aldrich), calcein-AM and propidium iodide (PI) staining (Sigma Aldrich), Alexa Fluor 488 phalloidin and 4′,6-diamidino-2-phenylindole, dihydrochloride (DAPI) staining (ThermoFisher).

    Techniques: Staining, Cell Culture