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c2 confocal microscope software  (Nikon)


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    Structured Review

    Nikon c2 confocal microscope software
    C2 Confocal Microscope 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/c1+confocal+software/C2%2B/pm40185699-120-14-13
    Average 99 stars, based on 1 article reviews
    c2 confocal microscope software - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Activation Assay:

    Article Title: Imaging protein dynamics in live mitotic cells
    Article Snippet: We have also performed photoactivation using a Nikon laser scanning confocal microscope (Nikon C1) equipped with a 100X 1.45NA objective lens. .. Photoactivation was performed using a 405nm laser; the area of activation was restricted using the Nikon C1 confocal software. ..

    Software:

    Article Title: Imaging protein dynamics in live mitotic cells
    Article Snippet: We have also performed photoactivation using a Nikon laser scanning confocal microscope (Nikon C1) equipped with a 100X 1.45NA objective lens. .. Photoactivation was performed using a 405nm laser; the area of activation was restricted using the Nikon C1 confocal software. ..

    Article Title: Brain-Derived Neurotrophic Factor Val66Met polymorphism interacts with adolescent stress to alter hippocampal interneuron density and dendritic morphology in mice.
    Article Snippet: A Nikon C1 confocal microscope with an Andor Zyla 4.2 sCMOS camera was used to capture images at 20x magnification and 3 μm step z-stacks. .. A maximum projection image was created from each stack using the Nikon C1 confocal software. .. Expression of markers and area measurements were determined using the FIJI ImageJ 1.52 g software.

    Article Title: Sex-specific spatial memory deficits in mice with a conditional TrkB deletion on parvalbumin interneurons.
    Article Snippet: Accepted Manuscript Title: Sex-specific spatial memory deficits in mice with a conditional TrkB deletion on parvalbumin interneurons Authors: Adrienne Mary Grech, Xin Du, Simon S Murray, Junhua Xiao, Rachel Anne Hill PII: S0166-4328(19)30533-9 DOI: https://doi.org/10.1016/j.bbr.2019.111984 Article Number: 111984 Reference: BBR 111984 To appear in: Behavioural Brain Research Received date: 4 April 2019 Revised date: 23 May 2019 Accepted date: 27 May 2019 Please cite this article as: Grech AM, Du X, Murray SS, Xiao J, Hill RA, Sex-specific spatial memory deficits in mice with a conditional TrkB deletion on parvalbumin interneurons, Behavioural Brain Research (2019), https://doi.org/10.1016/j.bbr.2019.111984 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.

    Article Title: PTK6 Regulates IGF-1-Induced Anchorage-Independent Survival
    Article Snippet: Confocal analyses were performed using the Nikon TE2000 microscope with the C1plus confocal microscope system equipped with krypton-argon (488 line) and HeNe (543 and 633 lines) lasers. .. Structures were analyzed with a 40×/1.3 objective and images were acquired using the Nikon C1 Confocal software. ..

    Article Title: Brain-Derived Neurotrophic Factor Val66Met polymorphism interacts with adolescent stress to alter hippocampal interneuron density and dendritic morphology in mice
    Article Snippet: A Nikon C1 confocal microscope with an Andor Zyla 4.2 sCMOS camera was used to capture images at 20x magnification and 3 μm step z-stacks. .. A maximum projection image was created from each stack using the Nikon C1 confocal software. .. Expression of markers and area measurements were determined using the FIJI ImageJ 1.52 g software.

    Article Title: TLR4 and TLR9 Expression in Different Phenotypes of Rhinitis
    Article Snippet: Brightness and contrast levels were evaluated using C1 software (Nikon) and the Adobe Photoshop 7.0 program (Abacus Concepts Inc., Berkeley, CA). .. Densitometric analysis was carried out on images collected with the same channel series settings by using the C1 confocal software (Nikon) and then submitted to densitometric analysis using 1D ImageJ software (Image J v1.43; NIH- http://rsb.info.nih.gov/ij/ ). ..

    Article Title: CysLT 2 receptors interact with CysLT 1 receptors and down-modulate cysteinyl leukotriene–dependent mitogenic responses of mast cells
    Article Snippet: Subcellular localization of the receptors was assessed using a Nikon TE2000-U inverted microscope with a Nikon C1 plus laser scanning confocal system (Melville, NY). .. Images were acquired through a 30-μm pinhole with a Nikon 60× Oil CFI Plan Apochromat objective and analyzed with Nikon EZ-C for Nikon C1 Confocal Software, Gold Version 3.40 build 691. .. The resolution was set for the highest possible given the objective and lasers according to the Nikon software (in most cases, 71 nm/pixel ± 1 nm).



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    For each oocyte, corresponding bright-field (A,B,C), UV light <t>(A1,B1,C1)</t> <t>and</t> <t>confocal</t> 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.
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    Nikon confocal acquisition software nikon ez c1 version 3 90
    For each oocyte, corresponding bright-field (A,B,C), UV light <t>(A1,B1,C1)</t> <t>and</t> <t>confocal</t> 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.
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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: