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dapi staining solution containing antifade mounting medium  (Servicebio Inc)

 
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    Structured Review

    Servicebio Inc dapi staining solution containing antifade mounting medium
    Dapi Staining Solution Containing Antifade Mounting Medium, supplied by Servicebio Inc, 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/dapi-containing+antifade+mounting+solution/dapi/pmc11191282-87-10-15
    Average 90 stars, based on 1 article reviews
    dapi staining solution containing antifade mounting medium - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Harnessing the gut–immune–joint axis: Oral microalgae-based thermoresponsive microspheres enhance intra-articular therapy for rheumatoid arthritis
    Article Snippet: After 2 h, basolateral samples were collected and fluorescence intensity was recorded (Ex/Em = 492/520 nm) using a microplate reader (SpectraMax iD5, Molecular Devices, USA). .. For tight junction (TJ) protein detection, Caco-2 monolayers were fixed and stained with antibodies against Claudin-1 (Abnova, China), Occludin (Abcam, UK), and ZO-1 (Abcam, UK), followed by DAPI (Servicebio, Wuhan, China) counterstaining. .. Fluorescence images were captured using a laser scanning confocal microscope and analyzed with ImageJ software.

    Article Title: Fabrication of RADA32/Ngf_EE/MSCs composite hydrogel and its protective mechanism against radiation-induced ototoxicity
    Article Snippet: After removal of the primary antibody, cells were incubated with a fluorescently labeled secondary antibody (AS039, ABclonal) at room temperature for 60 minutes protected from light. .. Finally, nuclei were stained with DAPI (G1012-10ML, Servicebio) for 10 minutes in the dark. ..

    Article Title: Sensory nerve-derived semaphorin 3A promotes bone healing through macrophage immunomodulation.
    Article Snippet: Sensory innervation has emerged as a crucial regulator of skeletal homeostasis and regeneration.. Growing evidence indicates that disruption of sensory nerves is associated with excessive inflammation and impaired tissue healing.. However, the underlying mechanisms by which neuronal signaling regulates the immune microenvironment to orchestrate bone repair remain unclear.

    Incubation:

    Article Title: A dual-functional hydrogel integrating adhesive and lubricating interfaces for mitochondrial protection–Driven cartilage regeneration
    Article Snippet: Rat chondrocytes (P1) were seeded in 24-well plates (5 × 10 4 cells per well) and cultured to ∼70–80% confluence, stimulated with LPS (10 μg mL −1 , 12 h) to induce an inflammatory phenotype, and then treated with hydrogel extracts (Hy, AdHy, AdHy@Pae) for 24 h. Cells were washed three times with PBS, fixed in 4% paraformaldehyde for 15 min, permeabilized with 0.1% Triton X-100 (Aladdin, T434386) for 10 min, and blocked with 5% BSA (Solarbio, SW3015) at room temperature for 1 h. Primary antibodies were applied overnight at 4 °C: COL2A1 (Proteintech, 28459-1-AP, 1:200), SOX9 (HUABIO, HA723548, 1:1000), MMP9 (HUABIO, ET1704-69, 1:200), and ADAMTS5 (HUABIO, HA722011, 1:100). .. After three PBS washes, fluorescent secondary antibodies (Servicebio, Alexa Fluor 488, GB25303; Alexa Fluor 594, GB28303) were incubated for 1 h in the dark, nuclei were counterstained with DAPI (1 μg mL −1 , 5 min, Servicebio, G1012), and images were acquired on a Nikon Eclipse C2 confocal microscope (Japan). ..

    Confocal:

    Article Title: A dual-functional hydrogel integrating adhesive and lubricating interfaces for mitochondrial protection–Driven cartilage regeneration
    Article Snippet: Rat chondrocytes (P1) were seeded in 24-well plates (5 × 10 4 cells per well) and cultured to ∼70–80% confluence, stimulated with LPS (10 μg mL −1 , 12 h) to induce an inflammatory phenotype, and then treated with hydrogel extracts (Hy, AdHy, AdHy@Pae) for 24 h. Cells were washed three times with PBS, fixed in 4% paraformaldehyde for 15 min, permeabilized with 0.1% Triton X-100 (Aladdin, T434386) for 10 min, and blocked with 5% BSA (Solarbio, SW3015) at room temperature for 1 h. Primary antibodies were applied overnight at 4 °C: COL2A1 (Proteintech, 28459-1-AP, 1:200), SOX9 (HUABIO, HA723548, 1:1000), MMP9 (HUABIO, ET1704-69, 1:200), and ADAMTS5 (HUABIO, HA722011, 1:100). .. After three PBS washes, fluorescent secondary antibodies (Servicebio, Alexa Fluor 488, GB25303; Alexa Fluor 594, GB28303) were incubated for 1 h in the dark, nuclei were counterstained with DAPI (1 μg mL −1 , 5 min, Servicebio, G1012), and images were acquired on a Nikon Eclipse C2 confocal microscope (Japan). ..

    Microscopy:

    Article Title: A dual-functional hydrogel integrating adhesive and lubricating interfaces for mitochondrial protection–Driven cartilage regeneration
    Article Snippet: Rat chondrocytes (P1) were seeded in 24-well plates (5 × 10 4 cells per well) and cultured to ∼70–80% confluence, stimulated with LPS (10 μg mL −1 , 12 h) to induce an inflammatory phenotype, and then treated with hydrogel extracts (Hy, AdHy, AdHy@Pae) for 24 h. Cells were washed three times with PBS, fixed in 4% paraformaldehyde for 15 min, permeabilized with 0.1% Triton X-100 (Aladdin, T434386) for 10 min, and blocked with 5% BSA (Solarbio, SW3015) at room temperature for 1 h. Primary antibodies were applied overnight at 4 °C: COL2A1 (Proteintech, 28459-1-AP, 1:200), SOX9 (HUABIO, HA723548, 1:1000), MMP9 (HUABIO, ET1704-69, 1:200), and ADAMTS5 (HUABIO, HA722011, 1:100). .. After three PBS washes, fluorescent secondary antibodies (Servicebio, Alexa Fluor 488, GB25303; Alexa Fluor 594, GB28303) were incubated for 1 h in the dark, nuclei were counterstained with DAPI (1 μg mL −1 , 5 min, Servicebio, G1012), and images were acquired on a Nikon Eclipse C2 confocal microscope (Japan). ..



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    Image Search Results


    Temperature-dependent incorporation of hTf-QDs is higher than HSA-QDs in A549 cells. Cells were co-incubated with hTf-QDs (red) and HSA-QDs (green) for 3 h. ( A ) Representative plot showing the frequency of the number of NPs per A549 cell (quantification of three independent experiments are shown in panels ( E , F )). ( B – D ) Representative fluorescence microscopy images using UV and transmission light simultaneously of A549 cells at 4 °C ( B ), 37 °C ( C ), and 16HB14o- cells at 37 °C ( D ). The co-localization of two HSA-QDs and hTf-QDs is visualized in yellow (arrow). DAPI-stained nuclei are shown in blue. ( E ) Box plot of HSA-QDs and hTf-QDs per A549 cell incubated at 4 °C or 37 °C during 3 h. The box comprises the 2nd and 3rd quartile of the data and the horizontal thick line defines the median. Outliers (>1.5× interquartile range are marked by diamonds). ( F ) Box plot of the average number of HSA-QDs and hTf-QD per 16HB14o- cell incubated at 37 °C for 3 h.

    Journal: Pharmaceutics

    Article Title: Two-Step Preparation of Protein-Decorated Biohybrid Quantum Dot Nanoparticles for Cellular Uptake

    doi: 10.3390/pharmaceutics15061651

    Figure Lengend Snippet: Temperature-dependent incorporation of hTf-QDs is higher than HSA-QDs in A549 cells. Cells were co-incubated with hTf-QDs (red) and HSA-QDs (green) for 3 h. ( A ) Representative plot showing the frequency of the number of NPs per A549 cell (quantification of three independent experiments are shown in panels ( E , F )). ( B – D ) Representative fluorescence microscopy images using UV and transmission light simultaneously of A549 cells at 4 °C ( B ), 37 °C ( C ), and 16HB14o- cells at 37 °C ( D ). The co-localization of two HSA-QDs and hTf-QDs is visualized in yellow (arrow). DAPI-stained nuclei are shown in blue. ( E ) Box plot of HSA-QDs and hTf-QDs per A549 cell incubated at 4 °C or 37 °C during 3 h. The box comprises the 2nd and 3rd quartile of the data and the horizontal thick line defines the median. Outliers (>1.5× interquartile range are marked by diamonds). ( F ) Box plot of the average number of HSA-QDs and hTf-QD per 16HB14o- cell incubated at 37 °C for 3 h.

    Article Snippet: For fluorescence microscopic visualization, the slides were covered with DAPI-containing antifade mounting solution (ProLong ® Gold antifade reagent, Invitrogen).

    Techniques: Incubation, Fluorescence, Microscopy, Transmission Assay, Staining

    Digitoxin-loaded hTf-QDs reduced A549 cell number. Left panel: Representative fluorescence microscopy images (20×) of 16HB14o- and A549 cells incubated for 48 h without (Control, ( A , B ) panels) or with hTf-QDs (( C , D ) panels). hTf-QDs are visualized in red and DAPI-stained nuclei are shown in blue. ( E ) Effect of hTf-QDs loaded with digitoxin (hTf-QDs-Dig) on 16HB14o- (green) and A549 (red) cells treated for 48 h. As a control, cells were incubated without hTf-QDs (Control) or in the presence of hTf-QDs without digitoxin (hTf-QDs). * indicates significative difference between treatments.

    Journal: Pharmaceutics

    Article Title: Two-Step Preparation of Protein-Decorated Biohybrid Quantum Dot Nanoparticles for Cellular Uptake

    doi: 10.3390/pharmaceutics15061651

    Figure Lengend Snippet: Digitoxin-loaded hTf-QDs reduced A549 cell number. Left panel: Representative fluorescence microscopy images (20×) of 16HB14o- and A549 cells incubated for 48 h without (Control, ( A , B ) panels) or with hTf-QDs (( C , D ) panels). hTf-QDs are visualized in red and DAPI-stained nuclei are shown in blue. ( E ) Effect of hTf-QDs loaded with digitoxin (hTf-QDs-Dig) on 16HB14o- (green) and A549 (red) cells treated for 48 h. As a control, cells were incubated without hTf-QDs (Control) or in the presence of hTf-QDs without digitoxin (hTf-QDs). * indicates significative difference between treatments.

    Article Snippet: For fluorescence microscopic visualization, the slides were covered with DAPI-containing antifade mounting solution (ProLong ® Gold antifade reagent, Invitrogen).

    Techniques: Fluorescence, Microscopy, Incubation, Staining