Tissue slices to be analysed for zinc staining at the light microscopical level were treated in accordance with the following two procedures, respectively: For light microscopical analyses of thick sections the slices were placed in a 30% solution of sucrose until they sank to the bottom of the glass.
SEM and light microscopy analyses of the dar1 SAM reveal an abnormal partitioning of meristematic domains, and mutations known to affect the SAM structure and function were found to interact with dar1.
Gross and light microscopic analyses of the eye and the IOL showed fragments of iris tissue attached to the haptics, pigment dispersion within the eye, with pigmented epithelial cells attached to the lens haptics and interruptions of the iris pigmented epithelial layers, and signs of corneal decompensation.
Gross and light microscopic analyses of the eye showed that if anterior and posterior capsule openings are well stretched around the optic of this IOL design, proliferative/regenerative material is potentially confined to the intercapsular space of the capsular bag remnant outside the optic rim.
Multi-angle light scattering analyses of the samples along the oligomerization process also showed that the average molecular weight was increasing as a function of time (figure 3, Table S1), with a decrease of the fraction of the dimeric species and the increase of that of the oligomers.
AFM microscopy and light scattering analyses of the positively charged lipid-like ac-A6K-CONH2, KA6-CONH2 peptide formulations showed individual nanovesicles.
Light microscopy analyses of immunofluorescence and epifluorescence samples were performed with a Leica DM 6000 B (Leica microsystems, Bensheim, Germany).
However, light microscopic analyses of CGNs following OGD (1.5 h)/ Reox (7 h) showed characteristic morphological changes: the neurons were round, smaller and translucent, with disintegration of processes.
Light microscopic analyses of CRC cells were subsequently continued for over a week, with daily addition of new medium and inhibitor, but without any apparent effect on cell viability, growth or morphology.
Interestingly, the octopaminergic/tyraminergic neurons do not seem to be directly postsynaptic to gustatory sensory neurons, as argued by light microscopical analyses of their branching patterns as well as from the site of expression of pre- and postsynaptic markers (Thum A, Université Fribourg, personal communication).
