Hi there! I am working to adapt miniscopes to image fluorescent beads injected into the vasculature as a proxy for blood flow velocity. Our colleagues have made some suggested modifications to our miniscope imaging that would optimize tracking of beads with their methods. From that, I am wondering what controls the magnification of the miniscope (which looks to be about 6x-7x), and are there ways to modify this? We would actually want to decrease the magnification to about a third of what it is currently, decreasing resolution but increasing the field of view, which would help with tracking of faster beads
Thanks so much!
Abby