Hi Peter,
We need more info:
1. What is the tissue(s)? Species?
2. What is the marker(s) in question?
3. Answer 1 and 2 with regard to the shared images?
4. What is the expected staining reaction?
5. Is there a control section placed on the same slide? If yes...
6. How does the
Hi,
A lab which does a lot of immuno work on tissue sections (both DAB and
fluorescent labelling) have run into issues with uniformity of antibody
staining. Some areas of the tissue just don’t label and it seems to be a very
clear line between the stained and unstained tissue. The tissue was
