I guess you've seen lots of examples of the labelling already, but here's a
web site with a nice confocal pic of a lucifer yellow filled granule neuron
from the rat. You can even follow the axon for quite some distance in their
paper I think.
<tehgabriel at web.de> wrote in message
news:1115894014.112677.152940 at f14g2000cwb.googlegroups.com...
> So far i have no experience with staining of cells e.g. cortical
> neurons. For a new set of experiments we thought it might be useful to
> start with this in order to discriminate certain morphological criteria
> (some dendritic projections, general shape of dendritic tree etc.). It
> seems that the most common methods for staining are via biocytine or
> via lucifer yellow. What are the advantages/disadvantages of these two
> So far as i know, lucifer yellow is very easy to use, requires no
> histochemical preparation but does not stain fine dendritic structures.
> Biocytine, on the other hand, allows a finer resolution but requires
> some histochemics after the recording.
> What do you think/is your experience?
>> Every tip or comment is appreciated.