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nis-elements real-time deconvolution two-dimensional software  (Nikon)


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    Nikon nis-elements real-time deconvolution two-dimensional software
    Nis Elements Real Time Deconvolution Two Dimensional Software, 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/two-dimensional+deconvolution/pm22374978-97-20-27
    Average 90 stars, based on 1 article reviews
    nis-elements real-time deconvolution two-dimensional software - by Bioz Stars, 2026-10
    90/100 stars

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    Software:

    Article Title: Correlated cryogenic fluorescence microscopy and electron cryo-tomography shows that exogenous TRIM5α can form hexagonal lattices or autophagy aggregates in vivo
    Article Snippet: The grids were imaged using a 60× extra-long working distance air objective (Nikon CFI S Plan Fluor ELWD 60×, NA 0.7, WD 2.62 to 1.8 mm). .. Images were recorded using a Neo 5.5 sCMOS camera (Andor Technology) using a two-dimensional (2D) real-time deblur deconvolution module in the NIS Elements software from AutoQuant (Nikon Instruments). ..

    Article Title: Increased Colocalization and Interaction Between Decidual Protein Kinase A and Insulin-like Growth Factor-Binding Protein-1 in Intrauterine Growth Restriction.
    Article Snippet: .. To confirm colocalization from our widefield imaging was real and not due to technical artifact, we performed two-dimensional deconvolution of images (Fig. 9C and F) using NIS Elements software (Nikon Instruments Inc; Melville, NY) and the automatic deconvolution algorithm. ..

    Imaging:

    Article Title: Increased Colocalization and Interaction Between Decidual Protein Kinase A and Insulin-like Growth Factor-Binding Protein-1 in Intrauterine Growth Restriction.
    Article Snippet: .. To confirm colocalization from our widefield imaging was real and not due to technical artifact, we performed two-dimensional deconvolution of images (Fig. 9C and F) using NIS Elements software (Nikon Instruments Inc; Melville, NY) and the automatic deconvolution algorithm. ..



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    cLTP-enhanced recycling facilitates TrkB-FL translocation into postsynaptic densities. A, Hippocampal neurons (18 DIV) were transfected with GFP and treated with various agents as indicated. Endogenous TrkB-FL stained by the Trk (C-14) antibody that recognizes the C terminus of Trk (catalog# sc-11; Santa Cruz Biotechnology) was labeled red. Arrowheads and arrows denote protrusions with and without TrkB in the spine head, respectively. Scale bars, 1 μm. B, Three types of TrkB-FL distribution in spines. Scale bars, 2 μm. C, Proportions of spines containing TrkB-FL in the indicated locations. Graphs represent means ± SEM (n = 116, 169, and 135 spines analyzed from 8, 8, and 10 neurons, respectively, *p < 0.05 relative to no BDNF control of each group, #p < 0.05, χ2 test. D, Coimmunofluorescence labeling of recycled TrkB and PSD-95 in neurons (9 DIV) transfected with pcDNA3.1 or pCAGIG-GFP-Rab11S25N. Hippocampal neurons were stained for recycled TrkB (green) and PSD-95 (red) with (left) or without (right) glycine stimulation. Blue indicates neurons expressing pcAGIG-GFP-Rab11S25N. Colocalization is indicated by white arrows. Scale bars, 10 μm. E, Quantification analysis of the colocalization of recycled TrkB-FL or TrkB.T1 with PSD-95 in D. Graphs represent means ± SEM (n ≥ 30 cells for each condition per experiment, ***p < 0.001 relative to its baseline, #p < 0.05, Student's t test). F, Quantification analysis of the clusters of PSD95. Images were taken using a 100× objective and two-dimensional <t>deconvolution</t> software (MetaMorph) was used.
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    Image Search Results


    cLTP-enhanced recycling facilitates TrkB-FL translocation into postsynaptic densities. A, Hippocampal neurons (18 DIV) were transfected with GFP and treated with various agents as indicated. Endogenous TrkB-FL stained by the Trk (C-14) antibody that recognizes the C terminus of Trk (catalog# sc-11; Santa Cruz Biotechnology) was labeled red. Arrowheads and arrows denote protrusions with and without TrkB in the spine head, respectively. Scale bars, 1 μm. B, Three types of TrkB-FL distribution in spines. Scale bars, 2 μm. C, Proportions of spines containing TrkB-FL in the indicated locations. Graphs represent means ± SEM (n = 116, 169, and 135 spines analyzed from 8, 8, and 10 neurons, respectively, *p < 0.05 relative to no BDNF control of each group, #p < 0.05, χ2 test. D, Coimmunofluorescence labeling of recycled TrkB and PSD-95 in neurons (9 DIV) transfected with pcDNA3.1 or pCAGIG-GFP-Rab11S25N. Hippocampal neurons were stained for recycled TrkB (green) and PSD-95 (red) with (left) or without (right) glycine stimulation. Blue indicates neurons expressing pcAGIG-GFP-Rab11S25N. Colocalization is indicated by white arrows. Scale bars, 10 μm. E, Quantification analysis of the colocalization of recycled TrkB-FL or TrkB.T1 with PSD-95 in D. Graphs represent means ± SEM (n ≥ 30 cells for each condition per experiment, ***p < 0.001 relative to its baseline, #p < 0.05, Student's t test). F, Quantification analysis of the clusters of PSD95. Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Journal: The Journal of Neuroscience

    Article Title: BDNF-Dependent Recycling Facilitates TrkB Translocation to Postsynaptic Density during LTP via a Rab11-Dependent Pathway

    doi: 10.1523/JNEUROSCI.3256-12.2013

    Figure Lengend Snippet: cLTP-enhanced recycling facilitates TrkB-FL translocation into postsynaptic densities. A, Hippocampal neurons (18 DIV) were transfected with GFP and treated with various agents as indicated. Endogenous TrkB-FL stained by the Trk (C-14) antibody that recognizes the C terminus of Trk (catalog# sc-11; Santa Cruz Biotechnology) was labeled red. Arrowheads and arrows denote protrusions with and without TrkB in the spine head, respectively. Scale bars, 1 μm. B, Three types of TrkB-FL distribution in spines. Scale bars, 2 μm. C, Proportions of spines containing TrkB-FL in the indicated locations. Graphs represent means ± SEM (n = 116, 169, and 135 spines analyzed from 8, 8, and 10 neurons, respectively, *p < 0.05 relative to no BDNF control of each group, #p < 0.05, χ2 test. D, Coimmunofluorescence labeling of recycled TrkB and PSD-95 in neurons (9 DIV) transfected with pcDNA3.1 or pCAGIG-GFP-Rab11S25N. Hippocampal neurons were stained for recycled TrkB (green) and PSD-95 (red) with (left) or without (right) glycine stimulation. Blue indicates neurons expressing pcAGIG-GFP-Rab11S25N. Colocalization is indicated by white arrows. Scale bars, 10 μm. E, Quantification analysis of the colocalization of recycled TrkB-FL or TrkB.T1 with PSD-95 in D. Graphs represent means ± SEM (n ≥ 30 cells for each condition per experiment, ***p < 0.001 relative to its baseline, #p < 0.05, Student's t test). F, Quantification analysis of the clusters of PSD95. Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Article Snippet: Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Techniques: Translocation Assay, Transfection, Staining, Labeling, Control, Expressing, Software