[Histonet] IHC staining intensity.
Rene J Buesa
rjbuesa <@t> yahoo.com
Wed Nov 30 07:02:41 CST 2005
Hi Louise:
Quantifying IHC staining intensity as an evaluation of the overall reaction
and epitope abundance has been used in several procedures and
consistency on several qualitative aspects of the sections have been identified
as the limiting parameter in several procedures.
There are several papers published in the Journal of Histotechnology that deal
with this aspect (15: 123-126, 1992; 18: 119-125,1995; 19:23-25,1996;
22:109-111,1999).
This year I have also published a paper in the JOH [Quantifying Quality: a
review and scale proposal; 28: 89-97, 2005) that, as the title indicates, deals
with this subject.
If you don't have access to my paper, you can e-mail me your FAX number
and I can send you a copy.
You are not "logic fuzzy" because there will be cases of cells that have lost
their "integrity" due to sectioning. The approach would be to define which cells
or parts of the cells are going to be measured, and only use them.
Rene J.
louise renton <louise.renton <@t> gmail.com> wrote:
Dear all,
I am currently in discussion with someone doing research who is using
a semi quantitative method of reporting stainig using INTENSITY of
cytoplasmic staining as a means of quantifying results. Staining for
a specific antibody is reported as ranging from zero to 3+. What I
would like to know is whether IHC intensity is influenced by the
thickness of the section. What I mean is, if staining is seen in a
whole cell, or one that has been bisected - will there not be a
variation in that one will appear darker when compared to the other?
Or is this variation minimal? Is my logic fuzzy?
I appreciate any input on this matter
best regards
Louise Renton
Bone Research Unit
University of the Witwatersrand
Johannesburg
South Africa
"....onwards through the fog!"
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