Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Hello,
I am interested in estimating the volume density of mitochondria in brine
shrimp embryos. The shell around the encysted embryos makes it difficult to
fix the embryos for EM, so I am looking for alternative methods. Somebody
in my lab suggested that I squish the embryos, label the mitochondria with
MitoTracker and use a point counting method to estimate # of mitochondria
in images taken with a confocal microscope.
Has anyone else tried anything remotely like this? If so do you have any
words of wisdom? So far I am having only limited success with this
technique.
Any assistance will be greatly appreciated.
Julie
Julie Reynolds
Graduate Research Assistant
Dept. of Biological Sciences
Louisiana State University
[log in to unmask]