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two-dimensional deconvolution capability  (MetaMorph Inc)

 
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    MetaMorph Inc two-dimensional deconvolution capability
    Two Dimensional Deconvolution Capability, supplied by MetaMorph Inc, 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/2d+deconvolution/pm16154216-71-8-11
    Average 90 stars, based on 1 article reviews
    two-dimensional deconvolution capability - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Spatial regulation of the KH domain RNA-binding protein Rnc1 mediated by a Crm1-independent nuclear export system in Schizosaccharomyces pombe.
    Article Snippet: Maximum merged images were generated from seven Z-stack images and subjected to 2D decomvolution (Original) using MetaMorph.

    Article Title: Nucleolin Interacts and Co-Localizes with Components of Pre-Catalytic Spliceosome Complexes
    Article Snippet: Nucleolin is an RNA binding protein that is involved in many post-transcriptional regulation steps of messenger RNAs in addition to its nucleolar role in ribosomal RNA transcription and assembly in pre-ribosomes.. Acetylated nucleolin was found to be associated with nuclear speckles and to co-localize with the splicing factor SC35.. Previous nuclear pull down of nucleolin identified several splicing components and factors involved in RNA polymerase II transcription associated with nucleolin.

    Article Title: An RNA-binding protein, RNP-1, protects microtubules from nocodazole and localizes to the leading edge during cytokinesis and cell migration in Dictyostelium cells
    Article Snippet: To image GFP-labeled proteins, z-stack images were taken of dividing or interphase cells, and the images were corrected using the MetaMorph 3D Deconvolution function.

    Article Title: KIF5B plays important roles in dendritic spine plasticity and dendritic localization of PSD95 and FMRP in the mouse cortex in vivo.
    Article Snippet: Images were processed by 2D-deconvolution in Metamorph software.

    Article Title: Plekhh1, a partner of myosin 1 and an effector of EphB2, controls the cortical actin network during cell repulsion.
    Article Snippet: Deconvolution was carried out by the 3D deconvolution Metamorph module with the fast iterative constrained PSFbased algorithm44.

    Software:

    Article Title: Budding Yeast Kinetochore Proteins, Chl4 and Ctf19, Are Required to Maintain SPB-Centromere Proximity during G1 and Late Anaphase
    Article Snippet: .. For and Figures S4 and S5 in , the 3D distance between centromere (GFP) and spindle pole (RFP) was obtained following Cui et al., after deconvolving the images using MetaMorph 2D deconvolution software (nearest neighbors algorithm) . ..

    Article Title: KIAA0040 enhances glioma growth by controlling the JAK2/STAT3 signalling pathway.
    Article Snippet: .. Image processing: The acquired images were processed using Metamorph 2D deconvolution software, which helps enhance the image quality and visualize subcellular details. ..

    Article Title: Mitochondrial division occurs concurrently with autophagosome formation but independently of Drp1 during mitophagy.
    Article Snippet: .. The images were analyzed by the 3D deconvolution module of Metamorph 7 software. .. EM The pep4Δ and pep4Δ/dnm1Δ strains were cultured in YPL medium to mid-log phase and then shifted to SD-N and cultured for 6 h. Cells were pelleted and cryoimmobilized by high-pressure freezing using a high-pressure freezing system (EM ICE; Leica Biosystems).



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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