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light sheet fluorescence microscopy  (Oxford Instruments)


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    Structured Review

    Oxford Instruments light sheet fluorescence microscopy
    Light Sheet Fluorescence Microscopy, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44266 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/light+sheet+fluorescence+microscopy/Imaris/pmc12088024-79-12-19
    Average 99 stars, based on 44266 article reviews
    light sheet fluorescence microscopy - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Software:

    Article Title: A Combined Computational Fluid Dynamics Modeling and Geometric Morphometrics Methods Approach to Quantifying Hemodynamic and Anatomical Features of Embryonic Chick Heart Anatomies Reconstructed from Light Sheet Fluorescence Microscopy Imaging
    Article Snippet: .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Article Title: An anatomically informed computational fluid dynamics modeling approach for quantifying hemodynamics in the developing heart
    Article Snippet: Chick embryos were imaged at the UNC Microscopy Services Laboratory using the LaVision BioTec Ultramicroscope II. .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Fluorescence:

    Article Title: A Combined Computational Fluid Dynamics Modeling and Geometric Morphometrics Methods Approach to Quantifying Hemodynamic and Anatomical Features of Embryonic Chick Heart Anatomies Reconstructed from Light Sheet Fluorescence Microscopy Imaging
    Article Snippet: .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Article Title: An anatomically informed computational fluid dynamics modeling approach for quantifying hemodynamics in the developing heart
    Article Snippet: Chick embryos were imaged at the UNC Microscopy Services Laboratory using the LaVision BioTec Ultramicroscope II. .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Article Title: The tracheal system of scutigeromorph centipedes and the evolution of respiratory systems of myriapods.
    Article Snippet: .. Data from light sheet fluorescence microscopy were converted into Imaris files (ImarisFileConverterx64, Version 9.2.0, BitPlane) and images processed using the Imaris software. .. Data from synchrotron andmicroCT scans were further processed using Amira 6.4 (Thermo Fischer).

    Article Title: Changes in DNA repair compartments and cohesin loss promote DNA damage accumulation in aged oocytes.
    Article Snippet: .. Quantification of lagging chromosomes and chromosome fragmentation Two colour imaging datasets of anaphase from light sheet fluorescence microscopy were reconstructed in Imaris (Bitplane). .. Minor translational and rotational drifts during image acquisition were corrected using Imaris, Bitplane.

    Microscopy:

    Article Title: A Combined Computational Fluid Dynamics Modeling and Geometric Morphometrics Methods Approach to Quantifying Hemodynamic and Anatomical Features of Embryonic Chick Heart Anatomies Reconstructed from Light Sheet Fluorescence Microscopy Imaging
    Article Snippet: .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Article Title: An anatomically informed computational fluid dynamics modeling approach for quantifying hemodynamics in the developing heart
    Article Snippet: Chick embryos were imaged at the UNC Microscopy Services Laboratory using the LaVision BioTec Ultramicroscope II. .. The Imaris (Bitplane, Oxford Instruments) File Converter software was used to convert light sheet fluorescence microscopy-generated TIFF files to Imaris files. ..

    Article Title: The tracheal system of scutigeromorph centipedes and the evolution of respiratory systems of myriapods.
    Article Snippet: .. Data from light sheet fluorescence microscopy were converted into Imaris files (ImarisFileConverterx64, Version 9.2.0, BitPlane) and images processed using the Imaris software. .. Data from synchrotron andmicroCT scans were further processed using Amira 6.4 (Thermo Fischer).

    Article Title: Changes in DNA repair compartments and cohesin loss promote DNA damage accumulation in aged oocytes.
    Article Snippet: .. Quantification of lagging chromosomes and chromosome fragmentation Two colour imaging datasets of anaphase from light sheet fluorescence microscopy were reconstructed in Imaris (Bitplane). .. Minor translational and rotational drifts during image acquisition were corrected using Imaris, Bitplane.

    Imaging:

    Article Title: Changes in DNA repair compartments and cohesin loss promote DNA damage accumulation in aged oocytes.
    Article Snippet: .. Quantification of lagging chromosomes and chromosome fragmentation Two colour imaging datasets of anaphase from light sheet fluorescence microscopy were reconstructed in Imaris (Bitplane). .. Minor translational and rotational drifts during image acquisition were corrected using Imaris, Bitplane.



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    (A) Decrease rate of the neuronal (NeuN+) density in the SP during postnatal development. (The density in each stage – in P0)/(the density in P0) x100. (n = 3 brains, n = 18 images) (B) Immunohistochemical images of the coronal sections of Lapr1-GFP mouse brain at P0 (left) and 8 weeks (right) (C) Area of SP/L6b is defined by Lpar1-GFP expression (μm 2 ) (n=3). (D) Photographs of 4%PFA fixed mouse brain in P0 (top) and 8 weeks (bottom) (E) Anteroposterior (AP) length of the brain excluding the cerebellum (cm) (n=3) (F) Series of horizontal sections of 8-weel old Lpar1-GFP mouse brain, imaged by Light sheet fluorescence <t>microscopy.</t> Sections were taken at 200μm intervals. White arrows indicate the Lpar1-GFP+ SP layer.
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    Image Search Results


    (A) Decrease rate of the neuronal (NeuN+) density in the SP during postnatal development. (The density in each stage – in P0)/(the density in P0) x100. (n = 3 brains, n = 18 images) (B) Immunohistochemical images of the coronal sections of Lapr1-GFP mouse brain at P0 (left) and 8 weeks (right) (C) Area of SP/L6b is defined by Lpar1-GFP expression (μm 2 ) (n=3). (D) Photographs of 4%PFA fixed mouse brain in P0 (top) and 8 weeks (bottom) (E) Anteroposterior (AP) length of the brain excluding the cerebellum (cm) (n=3) (F) Series of horizontal sections of 8-weel old Lpar1-GFP mouse brain, imaged by Light sheet fluorescence microscopy. Sections were taken at 200μm intervals. White arrows indicate the Lpar1-GFP+ SP layer.

    Journal: bioRxiv

    Article Title: Most early-born subplate neurons persist as Layer 6b neurons in the adult mouse neocortex

    doi: 10.1101/2025.11.20.689634

    Figure Lengend Snippet: (A) Decrease rate of the neuronal (NeuN+) density in the SP during postnatal development. (The density in each stage – in P0)/(the density in P0) x100. (n = 3 brains, n = 18 images) (B) Immunohistochemical images of the coronal sections of Lapr1-GFP mouse brain at P0 (left) and 8 weeks (right) (C) Area of SP/L6b is defined by Lpar1-GFP expression (μm 2 ) (n=3). (D) Photographs of 4%PFA fixed mouse brain in P0 (top) and 8 weeks (bottom) (E) Anteroposterior (AP) length of the brain excluding the cerebellum (cm) (n=3) (F) Series of horizontal sections of 8-weel old Lpar1-GFP mouse brain, imaged by Light sheet fluorescence microscopy. Sections were taken at 200μm intervals. White arrows indicate the Lpar1-GFP+ SP layer.

    Article Snippet: Cleared whole brain tissues were imaged by Light sheet microscopy (Olympus, MVX10-LS), and the z-axis interval was 4 μm in the P0 sample and 9 μm in the 8 weeks.

    Techniques: Immunohistochemical staining, Expressing, Fluorescence, Microscopy