zen black software package (Carl Zeiss)
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90
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Carl Zeiss
zen black software package
Zen Black Software Package, supplied by Carl Zeiss, 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/zen+black+software+package/axiovision+software/pm40414521-138-6-11
Average 90 stars, based on 1 article reviews
Zen Black Software Package, supplied by Carl Zeiss, 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/zen+black+software+package/axiovision+software/pm40414521-138-6-11
Average 90 stars, based on 1 article reviews
zen black software package - by Bioz Stars,
2026-09
90/100 stars
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Software:Article Title: Multiplex genomic tagging of mammalian ATG8s to study autophagy Article Snippet: .. Airyscan processing was performed using the Airyscan module in the commercial Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds. Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structuredillumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Article Title: Evolutionary adaptation and asymmetric inheritance of polyploid giant cancer cells in esophageal squamous cell carcinoma. Article Snippet: 24 Polyploid Giant Cancer Cells (PGCCs) play a critical role in tumor progression due to their 25 distinctive biological behaviors.. However, the mechanisms by which PGCCs regulate their 26 composition and structure to adapt to dynamic environments during their formation remain poorly 27 understood.. In this study, we used multicolor labeling of major organelles in esophageal squamous 28 cell carcinoma (ESCC) cells combined with highand super-resolution time-lapse imaging to 29 monitor induced PGCCs in three dimensions. Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640 nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structured-illumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Article Title: A new cellular platform for studying autophagy Article Snippet: .. Airyscan processing performed using the Airyscan module in the commercial Article Title: UBASH3B-mediated MRPL12 Y60 dephosphorylation inhibits LUAD development by driving mitochondrial metabolism reprogramming Article Snippet: The SIM images were performed using a commercial Zeiss microscope (ELYRA 7 with Lattice-SIM, Carl Zeiss Microimaging). .. A549 cells were seeded in a 20-mm Glass Bottom Cell Culture Dish (NEST) and incubated with 100 nM MitoTracker Red CMXRos in F12K medium at 37 °C for 30 min. SIM processing was performed using the SIM module in the Article Title: Three-dimensional cell culture conditions promoted the Mesenchymal-Amoeboid Transition in the Triple-Negative Breast Cancer cell line MDA-MB-231. Article Snippet: .. Control of the microscope and laser was facilitated by the Article Title: Multiplex Genomic Tagging of Mammalian ATG8s to Study Autophagy. Article Snippet: .. Airyscan processing was performed using the Airyscan module in the commercial Generated:Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds. Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structuredillumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640 nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structured-illumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Incubation:Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds. Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structuredillumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Article Title: Stabilization of membrane topologies by proteinaceous remorin scaffolds Article Snippet: For GUV experiments: Images were acquired by confocal fluorescence microscopy (Nikon Eclipse Ti-E inverted microscope using a Nikon A1R confocal laser scanning system with laser lines: 405 nm, 488 nm, 561 nm, 640 nm; 60x/1.49 oil immersion objective; Nikon Instruments, Inc.) and analyzed using the corresponding NIS Elements software (NIS Elements Confocal 5.20, Nikon Instruments, Inc.) and ImageJ (Fiji win64, Open source). .. Super resolution images were generated using an ELYRA7, structured-illumination-microscope with 3D Lattice SIM (Zeiss), equipped with a 63x/1.4 Oil DIC objective, a Pecon incubation chamber ensuring stable temperature and processed using the Article Title: UBASH3B-mediated MRPL12 Y60 dephosphorylation inhibits LUAD development by driving mitochondrial metabolism reprogramming Article Snippet: The SIM images were performed using a commercial Zeiss microscope (ELYRA 7 with Lattice-SIM, Carl Zeiss Microimaging). .. A549 cells were seeded in a 20-mm Glass Bottom Cell Culture Dish (NEST) and incubated with 100 nM MitoTracker Red CMXRos in F12K medium at 37 °C for 30 min. SIM processing was performed using the SIM module in the Cell Culture:Article Title: UBASH3B-mediated MRPL12 Y60 dephosphorylation inhibits LUAD development by driving mitochondrial metabolism reprogramming Article Snippet: The SIM images were performed using a commercial Zeiss microscope (ELYRA 7 with Lattice-SIM, Carl Zeiss Microimaging). .. A549 cells were seeded in a 20-mm Glass Bottom Cell Culture Dish (NEST) and incubated with 100 nM MitoTracker Red CMXRos in F12K medium at 37 °C for 30 min. SIM processing was performed using the SIM module in the Control:Article Title: Three-dimensional cell culture conditions promoted the Mesenchymal-Amoeboid Transition in the Triple-Negative Breast Cancer cell line MDA-MB-231. Article Snippet: .. Control of the microscope and laser was facilitated by the Microscopy:Article Title: Three-dimensional cell culture conditions promoted the Mesenchymal-Amoeboid Transition in the Triple-Negative Breast Cancer cell line MDA-MB-231. Article Snippet: .. Control of the microscope and laser was facilitated by the |