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Overview
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Automated Imaging
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 | Ease of UseThe Graphical Experimental Manager (GEM) of cellSens Dimension software offers fully automated multidimensional observation (X, Y, Z, T, wavelength, and positions) and eases experiment setup. To increase efficiency, you can define macro functions, such as executing deconvolution processing, in the GEM. |
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Precise, Reliable HardwareAutomated FocusingThe cellSens software’s multipoint focus map enables automated focusing across wide image areas with multiple objective lenses, making it easier to stay in focus while you navigate your samples. Bright, Uniform Fluorescence IlluminationThe fluorescence illuminator (IX3-RFALFE) incorporates a fly-eye lens system to distribute light evenly. The system provides bright and uniform illumination to the entire field of view, which is well-suited for image stitching applications. |   |
  | Well Plates Made SimpleThe Well Plate Navigator and Database solutions for cellSens software facilitate proper screening during an experiment. Together, they improve the efficiency of viewing and analyzing well plate images with a large amount of data. Information such as date, file name, or well plate number are easily selectable with icons, displaying any selection of captured images to be used for further analysis. These solutions also enable continuous analysis of selected images (the batch macro function) using the well plate GUI. |
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Rapid DeconvolutionOlympus cellSens Dimension software includes live 2D deblurring for preview and acquisition, enabling better focusing of thick specimens. For further detail enhancement, TruSight deconvolution is available to reassign out-of-focus light. TruSight uses a constrained iterative deconvolution algorithm to produce improved resolution, contrast, and dynamic range with industry-leading high speed through GPU processing. To improve experiment efficiency, deconvolution processing can be defined as a macro function in the GEM. |  Left: Without TruSight / Right: With TruSight |
   | Simplify Your WorkflowSuitable Objectives for Observation with Plastic VesselsLUCPLFLN series objectives and, in particular, the UCPLFLN20XPH (NA 0.7) objective are well-suited for observation using plastic dishes. The objectives enable high-resolution observation of the cell proliferation process and deliver improved contrast across a wide area. This gives you the flexibility to image through plastic-bottom dishes in addition to glass. *Image: iPS-cell expressing Nanog reporter (GFP) Image data courtesy of: Tomonobu Watanabe, Ph.D. Laboratory for Comprehensive Bioimaging, RIKEN Quantitative Biology Center |
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Advanced AnalysisImages can be easily converted to statistically relevant data with cellSens software. The software features region-of-interest, phase analysis, and cell counting capabilities. Export raw measurement data to Microsoft® Excel® software or a cellSens workbook with a single click. |
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ReferencesL. Kruger, et al. Ductular and proliferative response of esophageal submucosal glands in a porcine model of esophageal injury and repair. Gastrointestinal and Liver Physiology (June 1,2017). A. Urakami, et al. Development of a novel virus-like particle vaccine platform that mimics immature form of alphavirus. Clinical and Vaccine Immunology (May 17, 2017). A. S. Hasan, et al. Cardiosphere-derived cells facilitate heart repair by modulating M1/M2 macrophage polarization and neutrophil recruitment. PLoS ONE (October 20, 2016). S. McKenna, et al. Perinatal endotoxemia induces sustained hepatic COX-2 expression through an NFκB-dependent mechanism. Journal of Innate Immunity (April 29, 2016). D. H. Adams, et al. Data on keratin expression in human cells cultured with Australian native plant extracts. Data Brief (March 16, 2016). H. Doi, et al. Potency of umbilical cord blood- and Wharton’s jelly-derived mesenchymal stem cells for scarless wound healing. Scientific Reports (January 5, 2016). D. Seko, et al. μ-Crystallin controls muscle function through thyroid hormone action. The FASEB Journal (December 30, 2015). Y. Ono, et al. Muscle stem cell fate is controlled by the cell polarity protein Scrib. Cell Reports (February 24, 2015). |
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Specifications
| Microscope Frame | IX83P2ZF | |
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| Observation Method > Super Resolution | - | |
| Observation Method > Confocal | - | |
| Observation Method > Total Internal Reflection Fluorescence | - | |
| Observation Method > Fluorescence (Blue/Green Excitation) | ✓ | |
| Observation Method > Fluorescence (Ultraviolet Excitation) | ✓ | |
| Observation Method > Differential Interference Contrast (DIC) | ✓ | |
| Observation Method > Phase Contrast | ✓ | |
| Observation Method > Brightfield | ✓ | |
| Revolving Nosepiece > Motorized (6 position) | ✓ | |
| Focus > Motorized |
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| Focus > Z Drift Compensator | ✓ | |
| Observation Tubes > Widefield (FN 22) > Tilting Binocular | ✓ | |
| Illuminator > Transmitted Köhler Illuminator > LED Lamp | ✓ | |
| Illuminator > Transmitted Köhler Illuminator > 100 W Halogen Lamp | ✓ | |
| Illuminator > Fluorescence Illuminator > 100 W Mercury Lamp | ✓ | |
| Illuminator > Fluorescence Illuminator > Light Guide Illumination | ✓ | |
| Fluorescence Mirror Turret > Motorized (8 position) | ✓ | |
| Stage > Motorized | Contact your local sales representative to hear about motorized stage options | |
| Stage > Mechanical > IX3-SVR Mechanical Stage with Right Handle |
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| Stage > Mechanical > IX3-SVL Mechanical Stage with Left Short Handle |
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| Condenser > Motorized > Universal Condenser | W.D. 27 mm, NA 0.55, motorized aperture and polarizer | |
| Condenser > Manual > Universal Condenser | NA 0.55/ W.D. 27 mm | |
| Condenser > Manual > Ultra-Long Working Distance Condenser | NA 0.3/ W.D. 73.3 mm | |
| Confocal Scanner | - | |
| Super Resolution Processing | - | |
| Accessories | - | |
| Dimensions (W × D × H) | 323 (W) x 475 (D) x 706 (H) mm (IX83 microscope frame) | |
| Weight | Approx. 47kg (IX83P2ZF) |
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