nis elements microscope imaging software (Nikon)
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nis elements microscope imaging software
Nis Elements Microscope Imaging Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 39798 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nis+elements+microscope+imaging+software/NIS-Elements/pmc12958767-123-21-26
Average 99 stars, based on 39798 article reviews
Nis Elements Microscope Imaging Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 39798 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nis+elements+microscope+imaging+software/NIS-Elements/pmc12958767-123-21-26
Average 99 stars, based on 39798 article reviews
nis elements microscope imaging software - by Bioz Stars,
2026-10
99/100 stars
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Microscopy:Article Title: Iterative SCRaMbLE for engineering synthetic genome modules and chromosomes Article Snippet: Cultures were grown overnight (30 °C, 250 rpm) and visualised on a Nikon Eclipse Ti inverted microscope at 20x magnification and optical conf. .. Bright field (BF) images were captured using the Nikon Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: .. Imaging was performed using a Zeiss® confocal microscope and analyzed using the Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: Ultra-thin Sect. (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL ® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: Ultra-thin sections (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice Article Snippet: Then the cells were fixed with 4% paraformaldehyde +5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTM Gold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice. Article Snippet: Then the cellswerefixed with 4% paraformaldehyde+5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTMGold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: Hepatic cytochrome P450 endoplasmic reticulum-associated degradation (ERAD): Topological determinants and cellular partnerships that dictate the preferential P450 proteolytic sorting into macroautophagy rather than UPS Article Snippet: Laser inputs were provided by an Integrated Laser Engine (Spectral Applied Research) with coherent laser lines at 488 nm for SURF imaging and 405 nm for BFP imaging. .. Images were captured with exposure times of 2 sec and acquisition was managed using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: .. Imaging was performed using a Zeiss ® confocal microscope and analyzed using the Imaging:Article Title: Iterative SCRaMbLE for engineering synthetic genome modules and chromosomes Article Snippet: Cultures were grown overnight (30 °C, 250 rpm) and visualised on a Nikon Eclipse Ti inverted microscope at 20x magnification and optical conf. .. Bright field (BF) images were captured using the Nikon Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: .. Imaging was performed using a Zeiss® confocal microscope and analyzed using the Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: Ultra-thin Sect. (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL ® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: Ultra-thin sections (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice Article Snippet: Then the cells were fixed with 4% paraformaldehyde +5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTM Gold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice. Article Snippet: Then the cellswerefixed with 4% paraformaldehyde+5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTMGold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: Hepatic cytochrome P450 endoplasmic reticulum-associated degradation (ERAD): Topological determinants and cellular partnerships that dictate the preferential P450 proteolytic sorting into macroautophagy rather than UPS Article Snippet: Laser inputs were provided by an Integrated Laser Engine (Spectral Applied Research) with coherent laser lines at 488 nm for SURF imaging and 405 nm for BFP imaging. .. Images were captured with exposure times of 2 sec and acquisition was managed using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: .. Imaging was performed using a Zeiss ® confocal microscope and analyzed using the Software:Article Title: Iterative SCRaMbLE for engineering synthetic genome modules and chromosomes Article Snippet: Cultures were grown overnight (30 °C, 250 rpm) and visualised on a Nikon Eclipse Ti inverted microscope at 20x magnification and optical conf. .. Bright field (BF) images were captured using the Nikon Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: .. Imaging was performed using a Zeiss® confocal microscope and analyzed using the Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: Ultra-thin Sect. (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL ® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis. Article Snippet: Ultra-thin sections (60 nm) were cut and stained with uranyl acetate and lead citrate, then examined with a JEM-1010 JEOL® TEM. .. Ten random fields per group were analyzed for axon and myelin measurements (area, diameter, circularity, G-ratio, myelin width, axon/sheath ratio) using Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice Article Snippet: Then the cells were fixed with 4% paraformaldehyde +5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTM Gold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice. Article Snippet: Then the cellswerefixed with 4% paraformaldehyde+5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTMGold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: Hepatic cytochrome P450 endoplasmic reticulum-associated degradation (ERAD): Topological determinants and cellular partnerships that dictate the preferential P450 proteolytic sorting into macroautophagy rather than UPS Article Snippet: Laser inputs were provided by an Integrated Laser Engine (Spectral Applied Research) with coherent laser lines at 488 nm for SURF imaging and 405 nm for BFP imaging. .. Images were captured with exposure times of 2 sec and acquisition was managed using Article Title: The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis Article Snippet: .. Imaging was performed using a Zeiss ® confocal microscope and analyzed using the Laser-Scanning Microscopy:Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice Article Snippet: Then the cells were fixed with 4% paraformaldehyde +5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTM Gold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon Article Title: IFN-β and ARTS deficiency promote the generation of hyper-efferocytic Ly6C + macrophages in resolving inflammation in male mice. Article Snippet: Then the cellswerefixed with 4% paraformaldehyde+5% sucrose and stained with Hoechst (1:500; Molecular probes) and slides were mounted with SlowFadeTMGold Antifade Mounting (Molecular probes). .. The slides were imaged using Nikon A1-R confocal laser scanning microscope and engulfment of apoptotic cells was calculated using Nikon |