Bigger areas of a slide are being examined where neuron connections can be mapped. With the high-resolution objective used in general microscopy only smaller areas can be examined, but at lower resolution bigger FOVs can be viewed. Our microscopes use both of the advantageous properties, so bigger FOV is digitized with higher resolution.
It is highly important that these two aspects dominate in this field. Confocal technique combined with the quantitative evaluation made with QuanCenter and the visualization of structures built from slide sets through 3DView.