供应活细胞成像工作站

Technology Bright field and fluorescent live-cell images from various cell culture dishes are directly captured in a cell culture hood or even in an cell culture incubator. The compact design allows the installation of the device in a hood or an incubator preventing con*ination by maintaining a sterile environment. Juli is able to capture sequential time-lapse fluorescence and/or bright images, which can be converted to movie files. Growing live-cell movies can be generated even in cell-culture incubators. The software provides a fluorescent and bright cell merging function through user friendly image processing software with one click of a button.     Important features of the JuLITM smart fluorescent cell analyzer: All-in-one stand-alone systems The compact easy-to-use design allows the JuLI to be placed in a tissue culture hood or a culture incubator. The integrated display and the on-board computer allows to operate PC-free. Dark-room free Unlike a conventional microscope, fluorescence imaging can now be seen with  the room lights on, and out in the main laboratory area. Communication through wireless data transfer Utilizing Wi-Fi technology, all data (including images and movies) can be  transferred automatically to a PC. Connect with Smart phone With your Smart Phone (iPhone and Android Phone) and iPad a user can  connect to the system to check the cell status. Software Highlights: The touch screen user interface of the JuLI, Smart fluorescent-cell viewer provides new tools to expand cellular research through proprietary software. Insightful data can be acquired, such as proliferation assays.  Live cell imaging Bright field / Fluorescent cell images Time-lapse imaging Merged bright field / fluorescence images Applications     Fluorescence GFP images of 3 different cell types The NIH3T3, COS7 and C2C12 cells were transfected by the NEON transfection system using 0,5 mikrogram of the EGFP-N1 plasmid. Images were captured 24 hours after transfection. Birght field adipogenesis images Examples of the differentiated adipocyte images for 6, 11 and 21 days are shown. Bright field and fluorescence merged images: The U-2OS cells were transfected by Invitrogens NEON transfection system. 0,5 mikrogram of GFP-MLPH plasmid and GFP-Rab plasmid were used for transfection. The images were captured 24 hours after transfection. 标签：     上海市细胞成像工作站   上海市细胞成像工作站厂家
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供应活细胞成像工作站