
www.Usenet.com
| <-- __Chronological__ --> | <-- __Thread__ --> |
Does anyone know the solution of the "strong edge, weak/negative center" problem we have with some routinely processed immuno slides (from paraffin blocks)?
What we get on the edge is a _real_ staining, i.e. the cells that should stain do stain, and these that should not do not. The problems seems to affect more severly some antibodies (like DAKO LCA or CD20). People from the company know about it (it is not only ours), but offer no reasonable solution.
Z. Rudzki staff pathologist Jagiellonian Univ., Poland
| <-- __Chronological__ --> | <-- __Thread__ --> |