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multiphoton fluorescence microscope  (KU Leuven)

 
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    Structured Review

    KU Leuven multiphoton fluorescence microscope
    Multiphoton Fluorescence Microscope, supplied by KU Leuven, 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/multiphoton+microscope/multiphoton+fluorescence+microscope/pm18339709-365-19-8
    Average 90 stars, based on 1 article reviews
    multiphoton fluorescence microscope - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: Discovery of a cholecystokinin-gastrin-like signaling system in nematodes.
    Article Snippet: .. We acknowledge the Cell Imaging Core of the Katholieke Universiteit Leuven Impulse financing heavy equipment, for access to the multiphoton fluorescence microscope. ..

    Fluorescence:

    Article Title: Discovery of a cholecystokinin-gastrin-like signaling system in nematodes.
    Article Snippet: .. We acknowledge the Cell Imaging Core of the Katholieke Universiteit Leuven Impulse financing heavy equipment, for access to the multiphoton fluorescence microscope. ..

    Microscopy:

    Article Title: Discovery of a cholecystokinin-gastrin-like signaling system in nematodes.
    Article Snippet: .. We acknowledge the Cell Imaging Core of the Katholieke Universiteit Leuven Impulse financing heavy equipment, for access to the multiphoton fluorescence microscope. ..



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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