z stack imaging (Carl Zeiss)
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Carl Zeiss
z stack imaging
Z Stack Imaging, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 55 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/module/ZEN+Module+Z+Stack/pmc13695281-82-9-12
Average 94 stars, based on 55 article reviews
Z Stack Imaging, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 55 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/module/ZEN+Module+Z+Stack/pmc13695281-82-9-12
Average 94 stars, based on 55 article reviews
z stack imaging - by Bioz Stars,
2026-11
94/100 stars
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Related Articles
Software:Article Title: The ABL-MYC axis controls WIPI1-enhanced autophagy in lifespan extension Article Snippet: Image acquisition and analysis was performed in 96-well plates with glass bottom (Cellvis, P96-0-N) using a laser scanning microscope (LSM) 800 (Zeiss) and a C Plan-Apochromat 63x/1.4 oil differential interference contrast (DIC) objective. .. The automated image acquisition was carried out with the ‘tiles’ Article Title: Reprogramming reactive glia into interneurons reduces chronic seizure activity in a mouse model of mesial temporal lobe epilepsy Article Snippet: .. In order to acquire dentate gyrus overviews with high resolution, the Tile Scan Article Title: A Fat-Facets-Dscam1-JNK Pathway Enhances Axonal Growth in Development and after Injury Article Snippet: .. A maximum projection was created for each brain side and each image was quantified for GFP intensity using the “Image Analysis” Article Title: Relocation is the key to successful correlative fluorescence and scanning electron microscopy. Article Snippet: In this chapter the authors report on an automated hardware and software solution enabling swift correlative sample array mapping of fluorescently stained molecules within cells and tissues across length scales.. Samples are first observed utilizing widefield optical and fluorescence microscopy, followed by scanning electron microscopy, using calibration points on a dedicated sample-relocation holder.. We investigated HeLa cells in vitro, fluorescently labeled for monosialoganglioside one (GM-1), across both imaging platforms within tens of minutes of initial sample preparation. Article Title: The ABL-MYC axis controls WIPI1-enhanced autophagy in lifespan extension. Article Snippet: Image acquisition and analysis was performed in 96-well plates with glass bottom (Cellvis, P96-0-N) using a laser scanning microscope (LSM) 800 (Zeiss) and a C Plan-Apochromat 63x/1.4 oil differential interference contrast (DIC) objective. .. The automated image acquisition was carried out with the ‘tiles’ Article Title: Post-transcriptional modulation of Dscam1 enhances axonal growth in development and after injury Article Snippet: .. A maximum projection was created for each brain side and each image was quantified for GFP intensity using the ‘Image Analysis’ Fluorescence:Article Title: Relocation is the key to successful correlative fluorescence and scanning electron microscopy. Article Snippet: In this chapter the authors report on an automated hardware and software solution enabling swift correlative sample array mapping of fluorescently stained molecules within cells and tissues across length scales.. Samples are first observed utilizing widefield optical and fluorescence microscopy, followed by scanning electron microscopy, using calibration points on a dedicated sample-relocation holder.. We investigated HeLa cells in vitro, fluorescently labeled for monosialoganglioside one (GM-1), across both imaging platforms within tens of minutes of initial sample preparation. Electron Microscopy:Article Title: Relocation is the key to successful correlative fluorescence and scanning electron microscopy. Article Snippet: In this chapter the authors report on an automated hardware and software solution enabling swift correlative sample array mapping of fluorescently stained molecules within cells and tissues across length scales.. Samples are first observed utilizing widefield optical and fluorescence microscopy, followed by scanning electron microscopy, using calibration points on a dedicated sample-relocation holder.. We investigated HeLa cells in vitro, fluorescently labeled for monosialoganglioside one (GM-1), across both imaging platforms within tens of minutes of initial sample preparation. Solvent:Article Title: Relocation is the key to successful correlative fluorescence and scanning electron microscopy. Article Snippet: In this chapter the authors report on an automated hardware and software solution enabling swift correlative sample array mapping of fluorescently stained molecules within cells and tissues across length scales.. Samples are first observed utilizing widefield optical and fluorescence microscopy, followed by scanning electron microscopy, using calibration points on a dedicated sample-relocation holder.. We investigated HeLa cells in vitro, fluorescently labeled for monosialoganglioside one (GM-1), across both imaging platforms within tens of minutes of initial sample preparation. Marker:Article Title: Relocation is the key to successful correlative fluorescence and scanning electron microscopy. Article Snippet: In this chapter the authors report on an automated hardware and software solution enabling swift correlative sample array mapping of fluorescently stained molecules within cells and tissues across length scales.. Samples are first observed utilizing widefield optical and fluorescence microscopy, followed by scanning electron microscopy, using calibration points on a dedicated sample-relocation holder.. We investigated HeLa cells in vitro, fluorescently labeled for monosialoganglioside one (GM-1), across both imaging platforms within tens of minutes of initial sample preparation. |