Page 121 - Live-cellanalysis handbook
P. 121

Kinetic Neuroimmune Assays


           IncuCyte neuroimmune assays at a glance

           In order to measure microglia function over time, various   the chemotactic response is generated throughout the experiment.
           quantitative and qualitative assays are employed. IncuCyte    In addition, visual assessment of morphological changes associated
                                                        ®
           HD phase imaging allows for visual observation of activation-  with stimuli response as the membrane of the plate is optically
           associated morphology changes, giving detailed insight into   clear.
           cellular changes associated with neurodegenerative diseases.
                                                                  IncuCyte  Phagocytosis Assays enable real-time, automated
                                                                         ®
                  ®
           IncuCyte  Chemotaxis Assays are fully automated solutions to   analysis of both phagocytosis and efferocytosis within your cell
           quantify directional migration in response to a stimulus. Utilizing a   culture incubator. Using non-perturbing, pH sensitive fluorescent
           proprietary migration microplate, the IncuCyte  ClearView 96-Well   probes, visualization and quantification of phagocytosis can be
                                               ®
           Chemotaxis Plate, label-free analysis and precise quantification of   achieved in real-time over the entire assay time course.


             Shortcomings of Traditional Assays                   Live-Cell Imaging and Analysis Approaches

            •  Requires fixation and immunostaining steps.        •  Real-time, label-free measurement of chemotaxis migration
                                                                    without fixing, staining or cell scraping steps.
            •  Measurements at user-defined time points.          •  Real-time automated analysis in 96- or 384-well formats.
            •  Inability to visualize, confirm morphological changes.  •  Direct visualization of morphological changes associated with
                                                                    biological response.
            •  Requirement for large number of cells for single-point   •  Analyze sensitive and rare cells with a cell sparing, highly
              measurements.                                         reproducible 96- or 384-well assays.


















































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