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confocal microscope ez c1 2 20 software  (Nikon)


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    Nikon confocal microscope ez c1 2 20 software
    Confocal Microscope Ez C1 2 20 Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ez+c1+microscope+software/C2%2B/pm37678707-92-25-22
    Average 99 stars, based on 1 article reviews
    confocal microscope ez c1 2 20 software - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Microscopy:

    Article Title: Patients Lung Derived Tumoroids (PLDTs) to model therapeutic response.
    Article Snippet: After mounting the slides, slides were visualized with a Nikon Eclipse 2000-C1 confocal microscope and filters corresponding to the characteristics of the fluorochrome used, and the 20× and 60× immersion objectives. .. The images were then converted to Tiff format and analyzed using the Nikon EZ-C1 microscope software. ..

    Software:

    Article Title: Patients Lung Derived Tumoroids (PLDTs) to model therapeutic response.
    Article Snippet: After mounting the slides, slides were visualized with a Nikon Eclipse 2000-C1 confocal microscope and filters corresponding to the characteristics of the fluorochrome used, and the 20× and 60× immersion objectives. .. The images were then converted to Tiff format and analyzed using the Nikon EZ-C1 microscope software. ..



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    Image Search Results


    For each oocyte, corresponding bright-field (A,B,C), UV light (A1,B1,C1) and confocal laser scanning images showing mt distribution pattern (A2,B2,C2), intracellular ROS localization (A3,B3,C3) and mt/ROS merge (A4,B4,C4) are shown. Oocytes are representative of heterogeneous (pericortical/perinuclear; A), homogeneous (B) and abnormal (C) mitochondrial distribution pattern, respectively. Scale bar represents 60 µm.

    Journal: PLoS ONE

    Article Title: In Vitro Acute Exposure to DEHP Affects Oocyte Meiotic Maturation, Energy and Oxidative Stress Parameters in a Large Animal Model

    doi: 10.1371/journal.pone.0027452

    Figure Lengend Snippet: For each oocyte, corresponding bright-field (A,B,C), UV light (A1,B1,C1) and confocal laser scanning images showing mt distribution pattern (A2,B2,C2), intracellular ROS localization (A3,B3,C3) and mt/ROS merge (A4,B4,C4) are shown. Oocytes are representative of heterogeneous (pericortical/perinuclear; A), homogeneous (B) and abnormal (C) mitochondrial distribution pattern, respectively. Scale bar represents 60 µm.

    Article Snippet: In each individual oocyte, the fluorescence intensity was measured at the equatorial plane (plane no. 13), with the aid of the EZ-C1 Gold Version 3.70 software platform for Nikon C1 confocal microscope.

    Techniques: