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psf-based iterative 3d deconvolution module  (universal imaging inc)

 
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    universal imaging inc psf-based iterative 3d deconvolution module
    Psf Based Iterative 3d Deconvolution Module, supplied by universal imaging 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/deconvolution+module/psf+based+iterative+3d+deconvolution+module/pm19136951-164-40-48
    Average 90 stars, based on 1 article reviews
    psf-based iterative 3d deconvolution module - by Bioz Stars, 2026-10
    90/100 stars

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    other:

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    Article Snippet: altered in the cblF defect of vitamin B12 metabolism Frank Rutsch1, Susann Gailus1, Isabelle R Miousse2, Terttu Suormala3, Corinne Sagné4, Mohammad Reza Toliat5, Gudrun Nürnberg5, Tanja Wittkampf1, Insa Buers6, Azita Sharifi4, Martin Stucki7,8, Christian Becker5, Matthias Baumgartner7, Horst Robenek6, Thorsten Marquardt1, Wolfgang Höhne9, Bruno Gasnier4, David S Rosenblatt2, Brian Fowler3 & Peter Nürnberg5,10



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    ( A , B ) HUVEC were treated with histamine (100 µM, Sigma-Aldrich) or thrombin (1 U/ml, CalBiochem) for 10 min, or left untreated with equivalent volumes of vehicle (media) as controls. Cells were subsequently fixed, permeabilized and stained for plakoglobin, β-catenin, and VE-cadherin, all visualized in grayscale to ensure unbiased comparative analysis. Higher magnification images (63X) were acquired using a Zeiss LSM 980 confocal microscope equipped with an Airyscan detector ( A ), while lower magnification images (40X) were captured on a Zeiss LSM 880 confocal microscope ( B ). Scale bars, 25 µm.

    Journal: The EMBO Journal

    Article Title: Plakoglobin transmits tension across VE-cadherin for vascular leak formation and leukocyte diapedesis

    doi: 10.1038/s44318-026-00732-0

    Figure Lengend Snippet: ( A , B ) HUVEC were treated with histamine (100 µM, Sigma-Aldrich) or thrombin (1 U/ml, CalBiochem) for 10 min, or left untreated with equivalent volumes of vehicle (media) as controls. Cells were subsequently fixed, permeabilized and stained for plakoglobin, β-catenin, and VE-cadherin, all visualized in grayscale to ensure unbiased comparative analysis. Higher magnification images (63X) were acquired using a Zeiss LSM 980 confocal microscope equipped with an Airyscan detector ( A ), while lower magnification images (40X) were captured on a Zeiss LSM 880 confocal microscope ( B ). Scale bars, 25 µm.

    Article Snippet: Zeiss LSM 980 Airyscan acquisitions were processed with Airyscan Joint Deconvolution processing module in ZEN blue software (Zeiss) to improve signal-to-noise and spatial resolution; LSM 880 images were used without further deconvolution.

    Techniques: Staining, Microscopy