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vectashield antifade mounting medium with dapi  (Vector Laboratories)


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    Structured Review

    Vector Laboratories vectashield antifade mounting medium with dapi
    Vectashield Antifade Mounting Medium With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 21980 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+fade+vectashield+mounting+medium/VECTASHIELD+Antifade+Mounting+Medium+with+DAPI/custom%40h-1200%4042755103
    Average 98 stars, based on 21980 article reviews
    vectashield antifade mounting medium with dapi - by Bioz Stars, 2026-09
    98/100 stars

    Images

    Related Articles

    Gentle:

    Article Title: MUC16 promotes triple-negative breast cancer lung metastasis by modulating RNA-binding protein ELAVL1/HUR
    Article Snippet: Next day, the cells were washed with PBS (5 min, 3×) and then incubated with fluorescein isothiocyanate-conjugated anti-mouse and Texas red-conjugated anti-rabbit secondary antibodies (Jackson Immunoresearch Labs, Inc.) for 30 min at room temperature in the dark. .. Further the tissues were washed with PBS (5 min, 3×) with gentle shaking and finally mounted with an anti-fade vectashield mounting medium containing DAPI (Vector Laboratories, Burlingame, CA, USA). .. Images were acquired with the LSM710 microscope (Carl Zeiss GmbH, Jena, Germany).

    Article Title: MUC16 promotes triple-negative breast cancer lung metastasis by modulating RNA-binding protein ELAVL1/HUR.
    Article Snippet: Next day, the cells were washed with PBS (5 min, 3×) and then incubated with fluorescein isothiocyanate-conjugated anti-mouse and Texas red-conjugated anti-rabbit secondary antibodies (Jackson Immunoresearch Labs, Inc.) for 30 min at room temperature in the dark. .. Further the tissues were washed with PBS (5 min, 3×) with gentle shaking and finally mounted with an anti-fade vectashield mounting medium containing DAPI (Vector Laboratories, Burlingame, CA, USA). .. Images were acquired with the LSM710 microscope (Carl Zeiss GmbH, Jena, Germany).

    Immunofluorescence:

    Article Title: Muscle stem cell activation in response to acute injury is promoted by transient exposure to neutrophil elastase
    Article Snippet: Cryosections of injured and contralateral uninjured, or never injured TA muscles were obtained on a cryostat (Thermo Fisher) set a 10 μm thickness, -20 °C. .. Sections were permeabilized with PBS + 0.2% Triton X100 and the rest of the immunofluorescence carried out the same way as already described above for cells, with the only difference that at the end, slides were mounted with anti-fade VectaShield mounting medium (Vector Labs) and a thin glass coverslip (Fisher Scientific). ..

    Article Title: Ixazomib triggers autophagic degradation of MUC5AC/integrin-β4 and inhibits non-small cell lung cancer progression.
    Article Snippet: Background: Lung cancer is the most common cause of cancer-related deaths.. Despite recent advances in therapy, patients invariably develop resistance to standard treatments.. Hence, there is an increasing need to identify newer treatment approaches to enhance the efficacy of currently used agents and improve outcomes.

    Microscopy:

    Article Title: Rational design of an artificial tethered enzyme for non-templated post-transcriptional mRNA polyadenylation by the second generation of the C3P3 system
    Article Snippet: Cells were then incubated with the secondary Alexa Fluor 568-conjugated goat anti-rabbit A11036 orange-fluorescent (1:2000) and the Alexa Fluor 488-conjugated goat anti-mouse A11029 green-fluorescent antibody (1:500; Thermo-Fisher). .. Slides were mounted in the anti-fade Vectashield Mounting Medium (Vector Laboratories, Burlingame, CA), then imaged on a Leica SP8 confocal microscope equipped with the appropriate laser excitation filters under oil immersion with image magnification and processed with Leica LAS-AF software. ..

    Software:

    Article Title: Rational design of an artificial tethered enzyme for non-templated post-transcriptional mRNA polyadenylation by the second generation of the C3P3 system
    Article Snippet: Cells were then incubated with the secondary Alexa Fluor 568-conjugated goat anti-rabbit A11036 orange-fluorescent (1:2000) and the Alexa Fluor 488-conjugated goat anti-mouse A11029 green-fluorescent antibody (1:500; Thermo-Fisher). .. Slides were mounted in the anti-fade Vectashield Mounting Medium (Vector Laboratories, Burlingame, CA), then imaged on a Leica SP8 confocal microscope equipped with the appropriate laser excitation filters under oil immersion with image magnification and processed with Leica LAS-AF software. ..



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    Vector Laboratories anti fade mounting medium with dapi
    PT-PLATMC@PDA scaffold supports the survival, proliferation and spreading of cholangiocytes to form a monolayer. Cell viability (A) and density (B) of cholangiocytes seeded on PT-PLATMC@PDA films in culture for 1 day, 3 days, and 7 days (n = 3). Fluorescence microscope images of mouse liver derived cholangiocyte organoid seeded on the PT-PLATMC@PDA film in culture for 7 days (C), 14 days (D), 21 days (E) and 35 days (F) stained with <t>DAPI,</t> ZO-1, and CK19. DAPI and ECAD staining of the 21-day cultured mouse cholangiocytes (G) and 37-day cultured human cholangiocytes (H) seeded SMP PT-PLATMC@PDA planar films.
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    Vector Laboratories vectashield vibrance anti fade medium
    PT-PLATMC@PDA scaffold supports the survival, proliferation and spreading of cholangiocytes to form a monolayer. Cell viability (A) and density (B) of cholangiocytes seeded on PT-PLATMC@PDA films in culture for 1 day, 3 days, and 7 days (n = 3). Fluorescence microscope images of mouse liver derived cholangiocyte organoid seeded on the PT-PLATMC@PDA film in culture for 7 days (C), 14 days (D), 21 days (E) and 35 days (F) stained with <t>DAPI,</t> ZO-1, and CK19. DAPI and ECAD staining of the 21-day cultured mouse cholangiocytes (G) and 37-day cultured human cholangiocytes (H) seeded SMP PT-PLATMC@PDA planar films.
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    Image Search Results


    PT-PLATMC@PDA scaffold supports the survival, proliferation and spreading of cholangiocytes to form a monolayer. Cell viability (A) and density (B) of cholangiocytes seeded on PT-PLATMC@PDA films in culture for 1 day, 3 days, and 7 days (n = 3). Fluorescence microscope images of mouse liver derived cholangiocyte organoid seeded on the PT-PLATMC@PDA film in culture for 7 days (C), 14 days (D), 21 days (E) and 35 days (F) stained with DAPI, ZO-1, and CK19. DAPI and ECAD staining of the 21-day cultured mouse cholangiocytes (G) and 37-day cultured human cholangiocytes (H) seeded SMP PT-PLATMC@PDA planar films.

    Journal: Materials Today Bio

    Article Title: 4D fabrication of scaffolds facilitates the construction of cholangiocyte monolayers from human and mouse liver derived organoids

    doi: 10.1016/j.mtbio.2025.102757

    Figure Lengend Snippet: PT-PLATMC@PDA scaffold supports the survival, proliferation and spreading of cholangiocytes to form a monolayer. Cell viability (A) and density (B) of cholangiocytes seeded on PT-PLATMC@PDA films in culture for 1 day, 3 days, and 7 days (n = 3). Fluorescence microscope images of mouse liver derived cholangiocyte organoid seeded on the PT-PLATMC@PDA film in culture for 7 days (C), 14 days (D), 21 days (E) and 35 days (F) stained with DAPI, ZO-1, and CK19. DAPI and ECAD staining of the 21-day cultured mouse cholangiocytes (G) and 37-day cultured human cholangiocytes (H) seeded SMP PT-PLATMC@PDA planar films.

    Article Snippet: The samples were washed with PBS, mounted with 100 μl of anti-fade mounting medium with DAPI (Vector Laboratories Inc, USA), and analyzed under a confocal laser scanning microscope (Zeiss LSM880 with Ariyscan, Germany).

    Techniques: Fluorescence, Microscopy, Derivative Assay, Staining, Cell Culture

    Construction of a single-layer bile duct epithelium on PT-PLATMC@PDA tubular scaffolds. PT-PLATMC@PDA tubes seeded with (A) mouse derived cholangiocyte organoids cultured for 21 days and (B) human derived cholangiocyte organoids cultured for 37 days immuno-stained for DAPI, ZO-1and/or F Actin.

    Journal: Materials Today Bio

    Article Title: 4D fabrication of scaffolds facilitates the construction of cholangiocyte monolayers from human and mouse liver derived organoids

    doi: 10.1016/j.mtbio.2025.102757

    Figure Lengend Snippet: Construction of a single-layer bile duct epithelium on PT-PLATMC@PDA tubular scaffolds. PT-PLATMC@PDA tubes seeded with (A) mouse derived cholangiocyte organoids cultured for 21 days and (B) human derived cholangiocyte organoids cultured for 37 days immuno-stained for DAPI, ZO-1and/or F Actin.

    Article Snippet: The samples were washed with PBS, mounted with 100 μl of anti-fade mounting medium with DAPI (Vector Laboratories Inc, USA), and analyzed under a confocal laser scanning microscope (Zeiss LSM880 with Ariyscan, Germany).

    Techniques: Derivative Assay, Cell Culture, Staining