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stellaris5 point scanning microscope  (Danaher Inc)


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    Structured Review

    Danaher Inc stellaris5 point scanning microscope
    Stellaris5 Point Scanning Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/light+sheet+microscope/STELLARIS+DLS+Digital+Light+Sheet+Microscope/pm41362926-339-6-5
    Average 94 stars, based on 25 article reviews
    stellaris5 point scanning microscope - by Bioz Stars, 2026-09
    94/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: A chaperone-proteasome-based fragmentation machinery is essential for aggrephagy
    Article Snippet: Images were generated by collecting a stack of 6–16 images with focal planes 0.20 μm apart using a PLAPON ×60 oil, 1.42, WD 0.15 mm (Olympus) objective, and subsequently deconvolved using the SoftWoRx software (Applied Precision). .. Alternatively, confocal images were acquired using a SP8X DLS confocal/light-sheet microscope (Leica microsystems) with a HC PL APO CS2 ×63/1.4 oil objective. ..

    Article Title: Local mechanobiological disruption in solid tumor-driven vascular permeability: a competition between mechanical vs chemical stimuli.
    Article Snippet: .. Images were acquired with a confocal microscope (Leica, STELLARIS LightSheet (DLS)). ..

    Article Title: Local mechanobiological disruption in solid tumor-driven vascular permeability: a competition between mechanical vs chemical stimuli.
    Article Snippet: After 24 h, cells were exposed to the different media conditions described in Section 2.5 for 48 h. Afterwards, cells were fixed with 4% paraformaldehyde for 15 min at room temperature, permeabilized with 0.1% Triton X-100, and stained with anti-VE-Cadherin antibody (1:100, Santa Cruz). .. For morphological descriptors, fluorescence images were acquired using a confocal microscope (Leica, STELLARIS LightSheet (DLS)), and quantitative shape descriptors (cell area and circularity) were extracted using Cellpose detector plugins in ImageJ[42,43]. ..

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..

    Article Title: Control of Antibody Orientation on Graphene Using Porphyrin Linker Molecules for High-Performance Graphene-Based Immuno-Biosensors.
    Article Snippet: The appropriate orientation of antibodies on the graphene surface is critical for the high performance of graphene biosensors.. In this article, we show that a predominantly vertical orientation of antibodies to the graphene surface can be achieved by functionalizing the surface with tetrakis (4-carboxyphenyl) porphyrin (TCPP).. Unlike conventional pyrene-based linkers, such as 1pyrene butanoic acid succinimidyl ester (PBASE), which rely on a single flexible chain, the rigid porphyrin macrocycle of TCPP forms an extended π−π network with graphene and provides sites for uniform and directional antibody coupling.

    Article Title: A chaperone-proteasome-based fragmentation machinery is essential for aggrephagy.
    Article Snippet: Images were generated by collecting a stack of 6–16 images with focal planes 0.20 μm apart using a PLAPON ×60 oil, 1.42, WD 0.15 mm (Olympus) objective, and subsequently deconvolved using the SoftWoRx software (Applied Precision). .. Alternatively, confocal images were acquired using a SP8X DLS confocal/light-sheet microscope (Leica microsystems) with a HC PL APO CS2 ×63/1.4 oil objective. ..

    Imaging:

    Article Title: Light Sheet Microscopy Across Scales: From Single Cells to Whole Organs
    Article Snippet: Light sheet fluorescence microscopy (LSFM), or selective plane illumination microscopy (SPIM), has revolutionized biological imaging by enabling rapid, high-resolution 3D visualization of living and fixed specimens with minimal photodamage.. Since its introduction in 2004, LSFM has diversified into modalities suited for single-cell dynamics, small to medium tissues, and large, cleared specimens.. This article explores how different LSFM platforms are optimized for specific sample size ranges.

    Inverted Microscopy:

    Article Title: Light Sheet Microscopy Across Scales: From Single Cells to Whole Organs
    Article Snippet: Light sheet fluorescence microscopy (LSFM), or selective plane illumination microscopy (SPIM), has revolutionized biological imaging by enabling rapid, high-resolution 3D visualization of living and fixed specimens with minimal photodamage.. Since its introduction in 2004, LSFM has diversified into modalities suited for single-cell dynamics, small to medium tissues, and large, cleared specimens.. This article explores how different LSFM platforms are optimized for specific sample size ranges.

    Sample Prep:

    Article Title: Light Sheet Microscopy Across Scales: From Single Cells to Whole Organs
    Article Snippet: Light sheet fluorescence microscopy (LSFM), or selective plane illumination microscopy (SPIM), has revolutionized biological imaging by enabling rapid, high-resolution 3D visualization of living and fixed specimens with minimal photodamage.. Since its introduction in 2004, LSFM has diversified into modalities suited for single-cell dynamics, small to medium tissues, and large, cleared specimens.. This article explores how different LSFM platforms are optimized for specific sample size ranges.

    Fluorescence:

    Article Title: Local mechanobiological disruption in solid tumor-driven vascular permeability: a competition between mechanical vs chemical stimuli.
    Article Snippet: After 24 h, cells were exposed to the different media conditions described in Section 2.5 for 48 h. Afterwards, cells were fixed with 4% paraformaldehyde for 15 min at room temperature, permeabilized with 0.1% Triton X-100, and stained with anti-VE-Cadherin antibody (1:100, Santa Cruz). .. For morphological descriptors, fluorescence images were acquired using a confocal microscope (Leica, STELLARIS LightSheet (DLS)), and quantitative shape descriptors (cell area and circularity) were extracted using Cellpose detector plugins in ImageJ[42,43]. ..

    Software:

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..

    Spectrophotometry:

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..

    Article Title: Growing functional artificial cytoskeletons in the viscoelastic confinement of DNA synthetic cells
    Article Snippet: .. Software and code Policy information about availability of computer code Data collection Leica Stellaris5 Microscope (LAS X, v4.3.0.24308) ScanDrop spectrophotometer (Jena Analytic, FlashSoftPRO v1.2) DS-11 Spectrophotometer (DeNovix, v4.1.5) EVOS M7000 (Invitrogen, v2.1.677.717) Structured illumination microscopy (ZEISS Elyra 7) Atomic force microscopy (JPK SPM NanoWizard III) Intas Chemostar Touch 21.5 Gel Imager Data analysis ImageJ (v2.9.0; 64-bit) for image analysis Microsoft 365 Excel (Version 2307) for data analysis Origin 2023 (v10.0.0.154) for plot and fitting JPK Data Processing Software for analyzing the force profile of AFM data For manuscripts utilizing custom algorithms or software that are central to the research but not yet described in published literature, software must be made available to editors and reviewers. ..



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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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    (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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    (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