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inverted microscope leica dmi1  (Danaher Inc)


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    Structured Review

    Danaher Inc inverted microscope leica dmi1
    Inverted Microscope Leica Dmi1, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 98/100, based on 2217 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dmi1+inverted+microscope/DMi1+Inverted+Microscope/pmc12972718-339-6-8
    Average 98 stars, based on 2217 article reviews
    inverted microscope leica dmi1 - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Inverted Microscopy:

    Article Title: Effects of UVC-modified gallic acid (UVC-GA) on the quality and cytotoxicity of squid surimi
    Article Snippet: Fried foods are susceptible to quality deterioration and heterocyclic amine (HCA) formation during hightemperature processing.. Conventional antioxidants have limited efficacy, and research on improving the performance of natural antioxidants through photodynamic modification is insufficient.. In this study, gallic acid (GA) was irradiated with 225 nm ultraviolet C (UVC) for 6 h to prepare UVC-modified gallic acid (UVC-GA).

    Article Title: Stably-inverted organoids and methods of producing and using the same
    Article Snippet: Samples were coverslipped with Xylene and Cytoseal 60 (Richard-Allan Scientific). .. The samples were imaged using a DMi1 inverted microscope equipped with a color camera and 10× objective (Leica). .. Mounted sections were rinsed with PBS and permeabilized with 0.2% Triton X-100 (Sigma) for 5 minutes.



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    DFE induces apoptotic death in MCF7 and MDA-MB-231 cells, as observed by annexin V-propidium iodide (PI) dual staining. [ A.-D. ] Confocal images of MCF7 ( A ) and MDA-MB-231 ( C ) cells pre-treated with indicated doses of DFE (in µg/ml), DMSO, or doxorubicin (1.25 µM, as positive control) for 24 h were stained with annexin V and propidium iodide (PI) (laser scanning confocal <t>microscope</t> images through 63x oil lens). Hoechst 33342 stained the nuclei—scale bar- 25 µm. Bar graphs B and D represent the estimation of panels A and C, respectively. BF, bright fields. The dose-dependent increase of cell death was represented by a scatter plot based on LAS X analysis of the obtained images. Bar graphs representing the relative intensity of annexin V and propidium iodide (PI) in treatment groups. Error bar, mean ± SD ( n = 3); *P<0.05, **P <0.01, *** <0.001, ****P<0.0001.
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    Danaher Inc leica dmi1 microscope
    DFE induces apoptotic death in MCF7 and MDA-MB-231 cells, as observed by annexin V-propidium iodide (PI) dual staining. [ A.-D. ] Confocal images of MCF7 ( A ) and MDA-MB-231 ( C ) cells pre-treated with indicated doses of DFE (in µg/ml), DMSO, or doxorubicin (1.25 µM, as positive control) for 24 h were stained with annexin V and propidium iodide (PI) (laser scanning confocal <t>microscope</t> images through 63x oil lens). Hoechst 33342 stained the nuclei—scale bar- 25 µm. Bar graphs B and D represent the estimation of panels A and C, respectively. BF, bright fields. The dose-dependent increase of cell death was represented by a scatter plot based on LAS X analysis of the obtained images. Bar graphs representing the relative intensity of annexin V and propidium iodide (PI) in treatment groups. Error bar, mean ± SD ( n = 3); *P<0.05, **P <0.01, *** <0.001, ****P<0.0001.
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    Image Search Results


    DFE induces apoptotic death in MCF7 and MDA-MB-231 cells, as observed by annexin V-propidium iodide (PI) dual staining. [ A.-D. ] Confocal images of MCF7 ( A ) and MDA-MB-231 ( C ) cells pre-treated with indicated doses of DFE (in µg/ml), DMSO, or doxorubicin (1.25 µM, as positive control) for 24 h were stained with annexin V and propidium iodide (PI) (laser scanning confocal microscope images through 63x oil lens). Hoechst 33342 stained the nuclei—scale bar- 25 µm. Bar graphs B and D represent the estimation of panels A and C, respectively. BF, bright fields. The dose-dependent increase of cell death was represented by a scatter plot based on LAS X analysis of the obtained images. Bar graphs representing the relative intensity of annexin V and propidium iodide (PI) in treatment groups. Error bar, mean ± SD ( n = 3); *P<0.05, **P <0.01, *** <0.001, ****P<0.0001.

    Journal: Biotechnology Reports

    Article Title: Indole-alkaloid–rich fraction of Ervatamia coronaria leaf extract regresses breast cancer by inducing apoptotic cell death

    doi: 10.1016/j.btre.2025.e00937

    Figure Lengend Snippet: DFE induces apoptotic death in MCF7 and MDA-MB-231 cells, as observed by annexin V-propidium iodide (PI) dual staining. [ A.-D. ] Confocal images of MCF7 ( A ) and MDA-MB-231 ( C ) cells pre-treated with indicated doses of DFE (in µg/ml), DMSO, or doxorubicin (1.25 µM, as positive control) for 24 h were stained with annexin V and propidium iodide (PI) (laser scanning confocal microscope images through 63x oil lens). Hoechst 33342 stained the nuclei—scale bar- 25 µm. Bar graphs B and D represent the estimation of panels A and C, respectively. BF, bright fields. The dose-dependent increase of cell death was represented by a scatter plot based on LAS X analysis of the obtained images. Bar graphs representing the relative intensity of annexin V and propidium iodide (PI) in treatment groups. Error bar, mean ± SD ( n = 3); *P<0.05, **P <0.01, *** <0.001, ****P<0.0001.

    Article Snippet: Next, the images were taken with a Leica inverted microscope.

    Techniques: Staining, Positive Control, Microscopy