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counterstaining with dapi  (Beyotime)


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    Structured Review

    Beyotime counterstaining with dapi
    Counterstaining With Dapi, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 32308 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/counterstaining+with+dapi/DAPI/pm41981465-107-32-35
    Average 99 stars, based on 32308 article reviews
    counterstaining with dapi - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Blocking Assay:

    Article Title: ZFP36L1 promotes non-small cell lung cancer progression under hypoxia by modulating CXCL9:SPP1 polarity: A single-cell transcriptomic study.
    Article Snippet: For M0 macrophages, cells on sterile coverslips in 24- well plates were subjected to three PBS washings, 75% ethanol fixation (15 min) and .1% Triton X-100 (Beyotime) permeabilisation (15 min). .. After 1 h of 3% BSA (Beyotime) blocking, incubation with primary antibodies continued at 4◦C overnight; after PBS washings, at RT without lights, fluorophore-conjugated secondary antibodies were introduced for 1 h. After counterstaining with DAPI (Beyotime), nuclei were imaged with a fluorescence microscope (Olympus). .. For mouse tissues, sections were immobilised in 4% paraformaldehyde (PFA, Beyotime) for 24 h, dehydrated, embedded and sectioned into 5 μm.

    Article Title: An intelligent nanoliposome alleviates disc degeneration and discogenic pain by inhibiting neurovascular ingrowth via a “Soil-conditioning, seed-modulating, and weeds-suppressing” strategy
    Article Snippet: .. For immunofluorescence (IF) staining, antigen retrieval was conducted using citrate buffer (0.1 M, pH 6.0), followed by blocking in 10 % normal goat serum (Solarbio, Cat. No. SL038) at room temperature for 1 h. Sections were incubated overnight at 4 °C with primary antibodies targeting ACAN (Cat. No. DF7561, Affinity), COL2A1 (Cat. No. AF0135, Affinity), MMP3 (Cat. No. AF0217, Affinity), MMP13 (Cat. No. 18165-1-AP, Proteintech), CD31 (Cat. No. AF0077, Affinity), p-LATS1 (Cat. No. AF7170, Affinity), p-YAP (Cat. No. AF3328, Affinity), Tuj1 (Cat. No. 66375, Proteintech), CGRP (Cat. No. DF7386, Affinity), SP (Cat. No. DF7522, Affinity), and PGP9.5 (Cat. No. AF5490, Affinity) followed by incubation with appropriate fluorescent secondary antibodies for 2 h at room temperature and counterstaining with DAPI (Beyotime, Cat. No. C1006). .. Fluorescence images were acquired using a BX53 microscope (Olympus), and signal intensity was quantified with ImageJ software.

    Incubation:

    Article Title: ZFP36L1 promotes non-small cell lung cancer progression under hypoxia by modulating CXCL9:SPP1 polarity: A single-cell transcriptomic study.
    Article Snippet: For M0 macrophages, cells on sterile coverslips in 24- well plates were subjected to three PBS washings, 75% ethanol fixation (15 min) and .1% Triton X-100 (Beyotime) permeabilisation (15 min). .. After 1 h of 3% BSA (Beyotime) blocking, incubation with primary antibodies continued at 4◦C overnight; after PBS washings, at RT without lights, fluorophore-conjugated secondary antibodies were introduced for 1 h. After counterstaining with DAPI (Beyotime), nuclei were imaged with a fluorescence microscope (Olympus). .. For mouse tissues, sections were immobilised in 4% paraformaldehyde (PFA, Beyotime) for 24 h, dehydrated, embedded and sectioned into 5 μm.

    Article Title: Spatially Defined DNA Origami Cell Engagers for T and Natural Killer Cell-Mediated Immune Modulation.
    Article Snippet: Cell engagers have emerged as a promising approach for cancer immunotherapy, yet their efficacy is often limited by structural constraints in antibody valency and spatial configuration.. Here, we present a DNA origamibased platform for the precise spatial organization of antibodies, enabling the construction of tailored multivalent cell engagers to enhance antitumor immunity.. By modulating the composition, valency, and spatial arrangement of antibodies on a single DNA origami scaffold at the single-molecule level, we developed two types of cell engagers, T cell engagers and natural killer cell engagers, that effectively activate immune cells and improve tumor specificity.

    Article Title: GDPD5-CD55-EGFR competitive binding axis regulates radioresistance and lipid accumulation in rectal cancer.
    Article Snippet: .. After PBS washing, cells were incubated with BODIPY 493/503 (D3922, Thermo Fisher Scientific) for lipid droplet visualization, followed by nuclear counterstaining with DAPI (C1002, Beyotime) for 5 min. Critical precautions included avoiding antigen retrieval, detergent treatments, and cell drying throughout the procedure. ..

    Article Title: An intelligent nanoliposome alleviates disc degeneration and discogenic pain by inhibiting neurovascular ingrowth via a “Soil-conditioning, seed-modulating, and weeds-suppressing” strategy
    Article Snippet: .. For immunofluorescence (IF) staining, antigen retrieval was conducted using citrate buffer (0.1 M, pH 6.0), followed by blocking in 10 % normal goat serum (Solarbio, Cat. No. SL038) at room temperature for 1 h. Sections were incubated overnight at 4 °C with primary antibodies targeting ACAN (Cat. No. DF7561, Affinity), COL2A1 (Cat. No. AF0135, Affinity), MMP3 (Cat. No. AF0217, Affinity), MMP13 (Cat. No. 18165-1-AP, Proteintech), CD31 (Cat. No. AF0077, Affinity), p-LATS1 (Cat. No. AF7170, Affinity), p-YAP (Cat. No. AF3328, Affinity), Tuj1 (Cat. No. 66375, Proteintech), CGRP (Cat. No. DF7386, Affinity), SP (Cat. No. DF7522, Affinity), and PGP9.5 (Cat. No. AF5490, Affinity) followed by incubation with appropriate fluorescent secondary antibodies for 2 h at room temperature and counterstaining with DAPI (Beyotime, Cat. No. C1006). .. Fluorescence images were acquired using a BX53 microscope (Olympus), and signal intensity was quantified with ImageJ software.

    Article Title: Elucidating the Role of Oxidative Stress-Associated Genes FKBP Prolyl Isomerase 5 in Osteoarthritis Development and Immunological Milieu.
    Article Snippet: After removing the culture medium, cells were fixed with 4% paraformaldehyde (Biosharp, Hefei, China) for 10 minutes at ambient temperature and then rinsed three times with PBS (Gibco, Grand Island, NY, USA). .. The EdU detection procedure was conducted according to manufacturer specifications using the Click-iTTM EdU Imaging Kit (Invitrogen, Carlsbad, CA, USA): cells were incubated with EdU reaction mixture (light-protected environment) followed by nuclear counterstaining with DAPI (Beyotime Biotechnology, Shanghai, China). .. After final PBS washes, samples were visualized by a fluorescence microscope (Olympus, Tokyo, Japan).

    Fluorescence:

    Article Title: ZFP36L1 promotes non-small cell lung cancer progression under hypoxia by modulating CXCL9:SPP1 polarity: A single-cell transcriptomic study.
    Article Snippet: For M0 macrophages, cells on sterile coverslips in 24- well plates were subjected to three PBS washings, 75% ethanol fixation (15 min) and .1% Triton X-100 (Beyotime) permeabilisation (15 min). .. After 1 h of 3% BSA (Beyotime) blocking, incubation with primary antibodies continued at 4◦C overnight; after PBS washings, at RT without lights, fluorophore-conjugated secondary antibodies were introduced for 1 h. After counterstaining with DAPI (Beyotime), nuclei were imaged with a fluorescence microscope (Olympus). .. For mouse tissues, sections were immobilised in 4% paraformaldehyde (PFA, Beyotime) for 24 h, dehydrated, embedded and sectioned into 5 μm.

    Article Title: Photothermal reprogramming of synovial M1 macrophages reshapes the pro-inflammatory microenvironment to reverse temporomandibular joint osteoarthritis
    Article Snippet: .. Nuclei were visualized by counterstaining with DAPI (C1006, Beyotime) for 10 min. All fluorescence images were captured with a confocal laser scanning microscope (CLSM; A1 Nikon, Japan). ..

    Article Title: Extracellular Vesicle‐Mediated Nucleolin Transfer in Glioblastoma: A Targetable Axis Driving Blood‐Tumour Barrier Formation
    Article Snippet: .. After counterstaining with DAPI (Beyotime, CHN), confocal images were acquired using a confocal fluorescence microscope (Zeiss 980, DE). ..

    Microscopy:

    Article Title: ZFP36L1 promotes non-small cell lung cancer progression under hypoxia by modulating CXCL9:SPP1 polarity: A single-cell transcriptomic study.
    Article Snippet: For M0 macrophages, cells on sterile coverslips in 24- well plates were subjected to three PBS washings, 75% ethanol fixation (15 min) and .1% Triton X-100 (Beyotime) permeabilisation (15 min). .. After 1 h of 3% BSA (Beyotime) blocking, incubation with primary antibodies continued at 4◦C overnight; after PBS washings, at RT without lights, fluorophore-conjugated secondary antibodies were introduced for 1 h. After counterstaining with DAPI (Beyotime), nuclei were imaged with a fluorescence microscope (Olympus). .. For mouse tissues, sections were immobilised in 4% paraformaldehyde (PFA, Beyotime) for 24 h, dehydrated, embedded and sectioned into 5 μm.

    Article Title: Extracellular Vesicle‐Mediated Nucleolin Transfer in Glioblastoma: A Targetable Axis Driving Blood‐Tumour Barrier Formation
    Article Snippet: .. After counterstaining with DAPI (Beyotime, CHN), confocal images were acquired using a confocal fluorescence microscope (Zeiss 980, DE). ..

    Laser-Scanning Microscopy:

    Article Title: Photothermal reprogramming of synovial M1 macrophages reshapes the pro-inflammatory microenvironment to reverse temporomandibular joint osteoarthritis
    Article Snippet: .. Nuclei were visualized by counterstaining with DAPI (C1006, Beyotime) for 10 min. All fluorescence images were captured with a confocal laser scanning microscope (CLSM; A1 Nikon, Japan). ..

    Confocal Laser Scanning Microscopy:

    Article Title: Photothermal reprogramming of synovial M1 macrophages reshapes the pro-inflammatory microenvironment to reverse temporomandibular joint osteoarthritis
    Article Snippet: .. Nuclei were visualized by counterstaining with DAPI (C1006, Beyotime) for 10 min. All fluorescence images were captured with a confocal laser scanning microscope (CLSM; A1 Nikon, Japan). ..

    Immunofluorescence:

    Article Title: An intelligent nanoliposome alleviates disc degeneration and discogenic pain by inhibiting neurovascular ingrowth via a “Soil-conditioning, seed-modulating, and weeds-suppressing” strategy
    Article Snippet: .. For immunofluorescence (IF) staining, antigen retrieval was conducted using citrate buffer (0.1 M, pH 6.0), followed by blocking in 10 % normal goat serum (Solarbio, Cat. No. SL038) at room temperature for 1 h. Sections were incubated overnight at 4 °C with primary antibodies targeting ACAN (Cat. No. DF7561, Affinity), COL2A1 (Cat. No. AF0135, Affinity), MMP3 (Cat. No. AF0217, Affinity), MMP13 (Cat. No. 18165-1-AP, Proteintech), CD31 (Cat. No. AF0077, Affinity), p-LATS1 (Cat. No. AF7170, Affinity), p-YAP (Cat. No. AF3328, Affinity), Tuj1 (Cat. No. 66375, Proteintech), CGRP (Cat. No. DF7386, Affinity), SP (Cat. No. DF7522, Affinity), and PGP9.5 (Cat. No. AF5490, Affinity) followed by incubation with appropriate fluorescent secondary antibodies for 2 h at room temperature and counterstaining with DAPI (Beyotime, Cat. No. C1006). .. Fluorescence images were acquired using a BX53 microscope (Olympus), and signal intensity was quantified with ImageJ software.

    Staining:

    Article Title: An intelligent nanoliposome alleviates disc degeneration and discogenic pain by inhibiting neurovascular ingrowth via a “Soil-conditioning, seed-modulating, and weeds-suppressing” strategy
    Article Snippet: .. For immunofluorescence (IF) staining, antigen retrieval was conducted using citrate buffer (0.1 M, pH 6.0), followed by blocking in 10 % normal goat serum (Solarbio, Cat. No. SL038) at room temperature for 1 h. Sections were incubated overnight at 4 °C with primary antibodies targeting ACAN (Cat. No. DF7561, Affinity), COL2A1 (Cat. No. AF0135, Affinity), MMP3 (Cat. No. AF0217, Affinity), MMP13 (Cat. No. 18165-1-AP, Proteintech), CD31 (Cat. No. AF0077, Affinity), p-LATS1 (Cat. No. AF7170, Affinity), p-YAP (Cat. No. AF3328, Affinity), Tuj1 (Cat. No. 66375, Proteintech), CGRP (Cat. No. DF7386, Affinity), SP (Cat. No. DF7522, Affinity), and PGP9.5 (Cat. No. AF5490, Affinity) followed by incubation with appropriate fluorescent secondary antibodies for 2 h at room temperature and counterstaining with DAPI (Beyotime, Cat. No. C1006). .. Fluorescence images were acquired using a BX53 microscope (Olympus), and signal intensity was quantified with ImageJ software.

    Imaging:

    Article Title: Elucidating the Role of Oxidative Stress-Associated Genes FKBP Prolyl Isomerase 5 in Osteoarthritis Development and Immunological Milieu.
    Article Snippet: After removing the culture medium, cells were fixed with 4% paraformaldehyde (Biosharp, Hefei, China) for 10 minutes at ambient temperature and then rinsed three times with PBS (Gibco, Grand Island, NY, USA). .. The EdU detection procedure was conducted according to manufacturer specifications using the Click-iTTM EdU Imaging Kit (Invitrogen, Carlsbad, CA, USA): cells were incubated with EdU reaction mixture (light-protected environment) followed by nuclear counterstaining with DAPI (Beyotime Biotechnology, Shanghai, China). .. After final PBS washes, samples were visualized by a fluorescence microscope (Olympus, Tokyo, Japan).



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    (a) Actin (green) and <t>DAPI</t> (blue) stain of tendon derived cells seeded on tissue culture plate (TCP) monolayer controls, healthy mimetic models and diseased mimetic models ( n = 3). Scale bar: 100 μm. (b) Nuclear aspect ratio (NAR) was quantified using ImageJ by converting microscopic image to grayscale and measuring major and minor axes of individual nuclei. A higher major‐to‐minor ratio indicates increased cellular elongations. (c) Cells on the healthy model showed greater elongation than both the monolayer control and diseased model by day 3, while the diseased model also exceeded the monolayer control. By day 5, elongation remained elevated only in the healthy model relative to the diseased, and by day 7, the healthy group exhibited significantly greater elongation than all other models. No significant differences were observed by day 10. Significance was defined as p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****), ns = not significant.
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    Image Search Results


    (a) Actin (green) and DAPI (blue) stain of tendon derived cells seeded on tissue culture plate (TCP) monolayer controls, healthy mimetic models and diseased mimetic models ( n = 3). Scale bar: 100 μm. (b) Nuclear aspect ratio (NAR) was quantified using ImageJ by converting microscopic image to grayscale and measuring major and minor axes of individual nuclei. A higher major‐to‐minor ratio indicates increased cellular elongations. (c) Cells on the healthy model showed greater elongation than both the monolayer control and diseased model by day 3, while the diseased model also exceeded the monolayer control. By day 5, elongation remained elevated only in the healthy model relative to the diseased, and by day 7, the healthy group exhibited significantly greater elongation than all other models. No significant differences were observed by day 10. Significance was defined as p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****), ns = not significant.

    Journal: Bioengineering & Translational Medicine

    Article Title: Extracellular matrix microarchitecture modulates cellular behavior and extracellular vesicle phenotypes in biomimetic tendon models

    doi: 10.1002/btm2.70134

    Figure Lengend Snippet: (a) Actin (green) and DAPI (blue) stain of tendon derived cells seeded on tissue culture plate (TCP) monolayer controls, healthy mimetic models and diseased mimetic models ( n = 3). Scale bar: 100 μm. (b) Nuclear aspect ratio (NAR) was quantified using ImageJ by converting microscopic image to grayscale and measuring major and minor axes of individual nuclei. A higher major‐to‐minor ratio indicates increased cellular elongations. (c) Cells on the healthy model showed greater elongation than both the monolayer control and diseased model by day 3, while the diseased model also exceeded the monolayer control. By day 5, elongation remained elevated only in the healthy model relative to the diseased, and by day 7, the healthy group exhibited significantly greater elongation than all other models. No significant differences were observed by day 10. Significance was defined as p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****), ns = not significant.

    Article Snippet: Cellular morphology was assessed via actin staining (Invitrogen, Cat. No. A12379) and nuclear counterstaining with DAPI (Fisher Scientific, Cat. No. H‐1200‐10) ( n = 3).

    Techniques: Staining, Derivative Assay, Control