Plate reader that captures the decisive moments of living cells - Spark Cyto
It is a microplate reader capable of time-lapse imaging of live cells.
I want to analyze adherent cancer cells without detaching them. This is recommended for those who are struggling with co-culturing adherent cells (stromal cells) and suspended leukemic cells, as they cannot be detached for analysis. With our unique real-time imaging capabilities, you can assay without detaching adherent cells, preserving the surrounding environment of the cells. There is no need to detach cells for assays like in flow cytometry. Experimental results can be presented as heat plots. *For more details, please refer to the materials. Feel free to contact us.
basic information
**Features** ● Real-Time Imaging Function - Real-Time Experimental Control (REC) By analyzing data such as the state of cells and fluorescence imaging while conducting experiments, it is possible to perform assays at the appropriate timing. Additionally, by simultaneously analyzing the state of molecular interactions as a plate reader, comprehensive information about all cells can be obtained. ● Clear Imaging of the Entire Well It is possible to capture images of the entire well from 6 to 384 well plates. Since information about the cells present in a single well can be obtained, the reliability of the data is enhanced. Furthermore, with a unique tiling function, adjacent fields of view can be seamlessly combined into a single image, creating a clear picture. By minimizing the meniscus effect of the liquid surface, uniform brightness across the entire well can be achieved during imaging. ● Auto Focus Using a patent-pending LED-based auto focus system, high-quality image acquisition is made possible while maintaining high-speed scanning. *For more details, please refer to the materials. Feel free to contact us with any inquiries.*
Price range
Delivery Time
Applications/Examples of results
- I want to analyze adhesive cancer cells without detaching them. - I am co-culturing adhesive cells (stromal cells) and suspended cells (leukemia cells), so I cannot detach them for analysis. - I want to visualize biological phenomena using fluorescence imaging (such as gene expression induced by Dox) to evaluate the effects of anticancer drugs and inhibitors. - I want to investigate T cell clones that kill cancer cells in a co-culture of fluorescently labeled cancer cells and tumor-infiltrating T cells.
Detailed information
Related Videos
Line up（4）
| Model number | overview |
|---|---|
| Spark Cyto 300 | |
| Spark Cyto 400 | |
| Spark Cyto 500 | |
| Spark Cyto 600 |
