opera phenix plus high throughput microplate confocal imager (Revvity)
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Revvity
opera phenix plus high throughput microplate confocal imager
Opera Phenix Plus High Throughput Microplate Confocal Imager, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 2540 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/opera+phenix+high+content+confocal+imaging+system/Opera+Phenix+Plus+high-content+screening+system/pm42033519-108-9-16
Average 96 stars, based on 2540 article reviews
Opera Phenix Plus High Throughput Microplate Confocal Imager, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 2540 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/opera+phenix+high+content+confocal+imaging+system/Opera+Phenix+Plus+high-content+screening+system/pm42033519-108-9-16
Average 96 stars, based on 2540 article reviews
opera phenix plus high throughput microplate confocal imager - by Bioz Stars,
2026-09
96/100 stars
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Related Articles
Imaging:Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux. Article Snippet: Unless otherwise indicated, images were acquired with an LSM700 microscope with a Plan-Apochromat 63×/1.40 Oil DIC M27 objective and Zen 2010 software (all equipment and software from Carl Zeiss, Jena, Germany) and analyzed with Image J (Fiji) software. .. For live imaging, cells were treated for 10min with CellMaskTM Green dye (1:1000) at 37 °C, then treated with LysoTrackerTM DeepRed for 30min at 37 °C, washed three times in PBS, treated with a Hoechst33342 and then processed for live imaging with an Article Title: Lipid droplets accumulate and delay regulated cell death execution Article Snippet: After three washes in 0.1% Triton X-100 in PBS, secondary Alexa Fluor-conjugated antibodies (1:1000; Thermo Fisher Scientific, A11011, A11004, A21235, A21244, A31553) were applied together with BODIPY 493/503 (0.5 μg/mL; Thermo Fisher Scientific, D3922) and Hoechst 33342 (1 μg/mL; Biotium, 3656055). .. Cells were washed three times with PBS and imaged using the Article Title: Integrated multi-omics analysis of metabolome and transcriptome profiles during bovine adipocyte differentiation reveals functional divergence of FADS2 isoforms in lipid metabolism regulation Article Snippet: To investigate the cellular changes at different time points, nuclei were stained with DAPI (Solarbio, Beijing, China), while lipid droplets were labeled with BODIPY 493/503 (MedChemExpress, New Jersey, USA). .. Subsequently, the stained cells were imaged using the Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux Article Snippet: Unless otherwise indicated, images were acquired with an LSM700 microscope with a Plan-Apochromat 63×/1.40 Oil DIC M27 objective and Zen 2010 software (all equipment and software from Carl Zeiss, Jena, Germany) and analyzed with Image J (Fiji) software. .. For live imaging, cells were treated for 10 min with CellMask TM Green dye (1:1000) at 37 °C, then treated with LysoTracker TM DeepRed for 30 min at 37 °C, washed three times in PBS, treated with a Hoechst-33342 and then processed for live imaging with an Article Title: Pooled multicolour tagging for visualizing subcellular protein dynamics Article Snippet: .. Clones on the imaging plates were imaged after 24 h and 48 h with an Article Title: TMEM165 replenishes lysosomal Ca 2+ stores, protects cells against Ca 2+ overload, and mediates Ca 2+ -induced lysosomal H + leakage Article Snippet: Unless otherwise indicated, images were acquired with an LSM700 microscope with a Plan-Apochromat 63×/1.40 Oil DIC M27 objective and Zen 2010 software (all equipment and software from Carl Zeiss, Jena, Germany) and analyzed with Image J (Fiji) software. .. For live imaging, cells were treated for 10 min with CellMask TM Green dye (1:1000) at 37°C, then treated with LysoTracker TM DeepRed for 30 min at 37°C, washed three times in PBS, treated with a Hoechst-33342 and then processed for live imaging with an Article Title: Integrated multi-omics analysis of metabolome and transcriptome profiles during bovine adipocyte differentiation reveals functional divergence of FADS2 isoforms in lipid metabolism regulation. Article Snippet: To investigate the cellular changes at different time points, nuclei were stained with DAPI (Solarbio, Beijing, China), while lipid droplets were labeled with BODIPY 493/503 (MedChemExpress, New Jersey, USA). .. Subsequently, the stained cells were imaged using the Staining:Article Title: Integrated multi-omics analysis of metabolome and transcriptome profiles during bovine adipocyte differentiation reveals functional divergence of FADS2 isoforms in lipid metabolism regulation Article Snippet: To investigate the cellular changes at different time points, nuclei were stained with DAPI (Solarbio, Beijing, China), while lipid droplets were labeled with BODIPY 493/503 (MedChemExpress, New Jersey, USA). .. Subsequently, the stained cells were imaged using the Article Title: Integrated multi-omics analysis of metabolome and transcriptome profiles during bovine adipocyte differentiation reveals functional divergence of FADS2 isoforms in lipid metabolism regulation. Article Snippet: To investigate the cellular changes at different time points, nuclei were stained with DAPI (Solarbio, Beijing, China), while lipid droplets were labeled with BODIPY 493/503 (MedChemExpress, New Jersey, USA). .. Subsequently, the stained cells were imaged using the other:Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux. Article Snippet: Cytosolic Ca2+ For Ca2+ imaging with Fluo-4-AM, cells were stained with 3mM Fluo-4AM for 25min in DMEM (Thermo Fisher, 10567014). Clone Assay:Article Title: Pooled multicolour tagging for visualizing subcellular protein dynamics Article Snippet: .. Clones on the imaging plates were imaged after 24 h and 48 h with an |