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upright stellaris 8 multiphoton microscope  (Danaher Inc)


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    Structured Review

    Danaher Inc upright stellaris 8 multiphoton microscope
    Upright Stellaris 8 Multiphoton Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 96/100, based on 135 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multiphoton+microscope/STELLARIS+8+DIVE+Multiphoton+Microscope/pm42907582-458-6-11
    Average 96 stars, based on 135 article reviews
    upright stellaris 8 multiphoton microscope - by Bioz Stars, 2026-11
    96/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Tolvaptan-Loaded Tomato-Derived Nanovesicles: Characterization and Evaluation of Cytotoxicity, Wound Healing Potential and the Effects on Cyst Formation in Renal Cell Lines
    Article Snippet: .. Images were obtained using a Leica Stellaris 8 DIVE confocal and multiphoton microscope (Leica Microsystems GmbH, Germany). ..

    Article Title: Tolvaptan-Loaded Tomato-Derived Nanovesicles: Characterization and Evaluation of Cytotoxicity, Wound Healing Potential and the Effects on Cyst Formation in Renal Cell Lines
    Article Snippet: Cell nuclei were stained with 4′,6-diamidino-2-phenylindole (DAPI) (Thermo Fisher Scientific, 62248, USA), and LysoTracker Deep Red (Invitrogen, L12492 , USA) was used to stain lysosomes in MDCK cells. .. The results were visualized using a Leica Stellaris 8 DIVE confocal and multiphoton microscope (Leica Microsystems GmbH, Germany). ..

    Article Title: Macrophagic Ym1 orchestrates γδT cell-derived IL-17 production and keratinocyte functionality to mediate psoriasis-like skin inflammation
    Article Snippet: DAPI (Bioworld Technology, China) was used to stain the nuclei. .. The images were captured by multiphoton microscope (SP8 DIVE, Leica). .. Leica Las X3.5.7 software was employed for both acquisition and analysis of immunofluorescence staining.

    Article Title: Why are soft collagenous tissues so tough?
    Article Snippet: .. The sample, along with the frame and the glasses, is transferred into a multiphoton microscope (Leica SP8 DIVE) with a 25× objective lens immersed in water. ..

    Article Title: Investigating the impact of microcalcification size and volume on collagenous matrix and tissue mechanics using a tissue-engineered atherosclerotic cap model
    Article Snippet: .. A multiphoton microscope (TCS SP5 Confocal, Leica, Germany) with a Chameleon Ultra multiphoton laser (710–1,040 nm) (Coherent, USA) was used to visualize collagen architecture ( ) and HA particles. ..

    Article Title: Improved biostability of gold nanostars for enhanced intercellular interactions.
    Article Snippet: Gold nanostars (AuNS) have emerged as promising platforms for biosensing, bioimaging, and therapeutic applications due to their strong plasmonic enhancement and tunable optical properties.. However, their applications are hindered by stability issues in complex biological environments, affecting their interactions with biomolecules and cells.. To address this challenge, we employ advanced characterization techniques, including surface-enhanced Raman spectroscopy (SERS) to track the stability and intracellular fate of AuNS.

    Article Title: Modelling Atherosclerotic Plaque Cap Mechanics: Microcalcifications Reduce Mechanical Properties in Mesenchymal Stromal Cell-Based Model.
    Article Snippet: .. A multiphoton microscope (TCS SP5 Confocal, Leica, Germany) with a Chameleon Ultra multiphoton laser (710–1040nm) (Coherent, USA) was used to visualize collagen architecture and microcalcifications. ..

    Article Title: Why are soft collagenous tissues so tough?
    Article Snippet: .. The sample, along with the frame and the glasses, is transferred into a multiphoton microscope (Leica SP8 DIVE) with a 25× objective lens immersed in water. ..

    Imaging:

    Article Title: Improved biostability of gold nanostars for enhanced intercellular interactions.
    Article Snippet: Gold nanostars (AuNS) have emerged as promising platforms for biosensing, bioimaging, and therapeutic applications due to their strong plasmonic enhancement and tunable optical properties.. However, their applications are hindered by stability issues in complex biological environments, affecting their interactions with biomolecules and cells.. To address this challenge, we employ advanced characterization techniques, including surface-enhanced Raman spectroscopy (SERS) to track the stability and intracellular fate of AuNS.



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    Protective effects of hiPSC-EV treatment on structural integrity and viability of hAO during IRI. (A) Experimental timeline. (B-E) Representative bright-field images (4x magnifications, EVOS microscope) of hAO pre-ischemia, post-ischemia (16 hours) and different reperfusion phases, show onset of cellular degeneration (black arrows). The bottom row of each image highlights morphological damage. (F) Label-free imaging of hAO pre-ischemia and different reperfusion phases (6 and 24 hours) performed using <t>multiphoton</t> microscopy. (G) hAO viability assessed by cellular ATP-dependent luminescence (RLU) at each time point. Data are mean ± SD (n = 3). Samples without hiPSC-EV treatment: w/o hiPSC-EV. Samples with hiPSC-EV treatment: with hiPSC-EV. *p < 0.05 versus pre-ischemia (control); # p < 0.05 versus IRI without hiPSC-EV.
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    Image Search Results


    Protective effects of hiPSC-EV treatment on structural integrity and viability of hAO during IRI. (A) Experimental timeline. (B-E) Representative bright-field images (4x magnifications, EVOS microscope) of hAO pre-ischemia, post-ischemia (16 hours) and different reperfusion phases, show onset of cellular degeneration (black arrows). The bottom row of each image highlights morphological damage. (F) Label-free imaging of hAO pre-ischemia and different reperfusion phases (6 and 24 hours) performed using multiphoton microscopy. (G) hAO viability assessed by cellular ATP-dependent luminescence (RLU) at each time point. Data are mean ± SD (n = 3). Samples without hiPSC-EV treatment: w/o hiPSC-EV. Samples with hiPSC-EV treatment: with hiPSC-EV. *p < 0.05 versus pre-ischemia (control); # p < 0.05 versus IRI without hiPSC-EV.

    Journal: International Journal of Biological Sciences

    Article Title: Extracellular Vesicles from Human Induced Pluripotent Stem Cells Reduce Lung Ischemia-Reperfusion Injury via Cytoprotective Mechanisms in both 2D Cultures and a Human Airway Organoid Model

    doi: 10.7150/ijbs.134686

    Figure Lengend Snippet: Protective effects of hiPSC-EV treatment on structural integrity and viability of hAO during IRI. (A) Experimental timeline. (B-E) Representative bright-field images (4x magnifications, EVOS microscope) of hAO pre-ischemia, post-ischemia (16 hours) and different reperfusion phases, show onset of cellular degeneration (black arrows). The bottom row of each image highlights morphological damage. (F) Label-free imaging of hAO pre-ischemia and different reperfusion phases (6 and 24 hours) performed using multiphoton microscopy. (G) hAO viability assessed by cellular ATP-dependent luminescence (RLU) at each time point. Data are mean ± SD (n = 3). Samples without hiPSC-EV treatment: w/o hiPSC-EV. Samples with hiPSC-EV treatment: with hiPSC-EV. *p < 0.05 versus pre-ischemia (control); # p < 0.05 versus IRI without hiPSC-EV.

    Article Snippet: Label-free imaging of hAO was also performed using a multiphoton microscopy Leica Stellaris DIVE 8 (Leica Microsystems, Germany), enabling visualization of cellular structures and intrinsic properties while maintaining the native organoid environment.

    Techniques: Microscopy, Label-free Imaging, Control