Expert articles & tutorials
We are pleased to share here with you our expertise and ideas in the field of control and image acquisition for fluorescence microscopes.
You will also find scientific publications that cite Inscoper in the Materials & Methods section.
To make it even easier for you to use our solutions, we regularly publish tutorials on various tips and tricks.
You are welcome to leave us your comments and share items you have liked.
FRAP experiment, 3 sequences
FRAP experiments are available to Inscoper users via the Photomanipulation dimension. In this video, we sequentially acquire 3 sequences (before FRAP, during FRAP, and after FRAP) and process data with visualization features. The cells used are U2OS cells, transfected...
Image Acquisition & Tiling
The Tiling feature included in the INSCOPER Microscopy Imaging Solution is used to image an entire slide (or well) or a large region of interest in the sample. Several images are acquired one after one in a row, called “tiles”, then “stitched” afterward to constitute...
FRAP Calibration
For the optimal use of the Photomanipulation Dimension of the INSCOPER Imaging Software, it is recommended to calibrate the laser in order to match up the position of the scanner optical head with the camera screen size. The microscope system is equipped with FRAP...
Image acquisition software is the microscope’s brain
Fluorescence microscopy has been a genuinely disruptive innovation for examining live specimens. It has enabled the invention of numerous imaging techniques and methods for observing the behaviour of biological objects of interest in a way that mirrors their spatial...
How to set time lapse
The procedure is as follows: Adjust the clarity of the image. Select a channel or add a new one. Determine the number of time points. Set an interval between each time point – >Total time will be calculated automatically. If other settings are not needed, disable...
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