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deconvolution software nikon software (nis-elements ar, nikon)  (Nikon)


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    Nikon deconvolution software nikon software (nis-elements ar, nikon)
    Deconvolution Software Nikon Software (Nis Elements Ar, Nikon), supplied by Nikon, 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/nikon+elements+deconvolution+software/pm37488906-131-2-7
    Average 90 stars, based on 1 article reviews
    deconvolution software nikon software (nis-elements ar, nikon) - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: Adult hippocampal MeCP2 preserves the genomic responsiveness to learning required for long-term memory formation.
    Article Snippet: Accepted Manuscript Adult hippocampal MeCP2 preserves the genomic responsiveness to learning required for long-term memory formation Kubra Gulmez Karaca, David V.C.. Brito, Benjamin Zeuch, Ana M.M.. Oliveira PII: S1074-7427(18)30029-7 DOI: https://doi.org/10.1016/j.nlm.2018.02.010 Reference: YNLME 6802 To appear in: Neurobiology of Learning and Memory Received Date: 24 November 2017 Revised Date: 4 February 2018 Accepted Date: 9 February 2018 Please cite this article as: Gulmez Karaca, K., Brito, D.V.C., Zeuch, B., Oliveira, A.M.M., Adult hippocampal MeCP2 preserves the genomic responsiveness to learning required for long-term memory formation, Neurobiology of Learning and Memory (2018), doi: https://doi.org/10.1016/j.nlm.2018.02.010 This is a PDF file of an unedited manuscript that has been accepted for publication.

    other:

    Article Title: The effect of single-cell knockout of Fragile X Messenger Ribonucleoprotein on synaptic structural plasticity
    Article Snippet: In vivo imaging of dendritic spines through the cranial window was performed on a two-photon microscope (Ultima Investigator, Bruker Co., Middleton, WI, USA) using a 16x/0.8 NA water-immersion objective (Nikon Instruments, Inc., Melville, NY, USA) and an ultrafast two-photon laser (Mai Tai, Spectra-Physics, Santa Clara, CA, USA) operating at 940 nm wavelength.

    Software:

    Article Title: Ethanol changes Nestin-promoter induced neural stem cells to disturb newborn dendritic spine remodeling in the hippocampus of mice.
    Article Snippet: The projection images were semiautomatically traced by ImageJ software with the Neuron J plugin. .. Images of dendritic spines were deconvoluted with Nikon Software (NIS-Elements AR, Nikon). ..



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    Image Search Results


    A). Maximum intensity projection and 3D volume projection images for OV4 EV and OE cells treated with or without EGF for 30 minutes. Images were obtained using 3D widefield-deconvolution microscopy. The images depict the distribution of EGFR (green) and Rab11 (magenta) obtained following the processing of the acquired widefield 3D Z-stack images by the Richardson-Lucy algorithm for deconvolution. Scale bar for the field of view (FOV) = 20 μm, region of interest (ROI) = 5 μm. B). Quantification of the fraction of EGFR co-localized with Rab11-positive endosomes was executed using the JACoP plugin in Fiji. Graphs depict mean +/− S.D. from two independent experiments with 20 cells analyzed per group, per experiment. Data were analyzed by one way ANOVA with Tukey’s test (ns: p > 0.05, ****: p < 0.0001).

    Journal: bioRxiv

    Article Title: Sialylation of EGFR by ST6GAL1 induces receptor activation and modulates trafficking dynamics

    doi: 10.1101/2023.06.03.543566

    Figure Lengend Snippet: A). Maximum intensity projection and 3D volume projection images for OV4 EV and OE cells treated with or without EGF for 30 minutes. Images were obtained using 3D widefield-deconvolution microscopy. The images depict the distribution of EGFR (green) and Rab11 (magenta) obtained following the processing of the acquired widefield 3D Z-stack images by the Richardson-Lucy algorithm for deconvolution. Scale bar for the field of view (FOV) = 20 μm, region of interest (ROI) = 5 μm. B). Quantification of the fraction of EGFR co-localized with Rab11-positive endosomes was executed using the JACoP plugin in Fiji. Graphs depict mean +/− S.D. from two independent experiments with 20 cells analyzed per group, per experiment. Data were analyzed by one way ANOVA with Tukey’s test (ns: p > 0.05, ****: p < 0.0001).

    Article Snippet: The widefield Z-stack images were deconvolved using Nikon Elements deconvolution software (Richardson Lucy; parameters: 50 iterations, low noise level).

    Techniques: Microscopy

    A). Maximum intensity projection and 3D volume projection images for OV4 EV and OE cells treated with or without EGF for 60 minutes. Cells were visualized by 3D widefield-deconvolution microscopy. The images depict the distribution of EGFR (green) and LAMP1 (magenta) obtained following the processing of the acquired widefield 3D Z-stack images by the Richardson-Lucy algorithm for deconvolution. Scale bar for the field of view (FOV) = 20 μm, region of interest (ROI) = 5 μm. B). Quantification of the fraction of EGFR co-localized with LAMP1-positive lysosomes was executed using the JACoP plugin in Fiji. Graphs depict mean +/− S.D. from two independent experiments with 20 cells analyzed per group, per experiment. Data were analyzed by one way ANOVA with Tukey’s test (ns: p > 0.05, ****: p < 0.0001).

    Journal: bioRxiv

    Article Title: Sialylation of EGFR by ST6GAL1 induces receptor activation and modulates trafficking dynamics

    doi: 10.1101/2023.06.03.543566

    Figure Lengend Snippet: A). Maximum intensity projection and 3D volume projection images for OV4 EV and OE cells treated with or without EGF for 60 minutes. Cells were visualized by 3D widefield-deconvolution microscopy. The images depict the distribution of EGFR (green) and LAMP1 (magenta) obtained following the processing of the acquired widefield 3D Z-stack images by the Richardson-Lucy algorithm for deconvolution. Scale bar for the field of view (FOV) = 20 μm, region of interest (ROI) = 5 μm. B). Quantification of the fraction of EGFR co-localized with LAMP1-positive lysosomes was executed using the JACoP plugin in Fiji. Graphs depict mean +/− S.D. from two independent experiments with 20 cells analyzed per group, per experiment. Data were analyzed by one way ANOVA with Tukey’s test (ns: p > 0.05, ****: p < 0.0001).

    Article Snippet: The widefield Z-stack images were deconvolved using Nikon Elements deconvolution software (Richardson Lucy; parameters: 50 iterations, low noise level).

    Techniques: Microscopy