Jm. Elias et M. Margiotta, LOW-TEMPERATURE ANTIGEN RESTORATION OF STEROID-HORMONE RECEPTOR PROTEINS IN ROUTINE PARAFFIN SECTIONS, Journal of histotechnology, 20(2), 1997, pp. 155-158
The most widely used non-enzymatic method for unmasking antigens prior
to immunohistochemical staining is based on immersion of deparaffiniz
ed paraffin sections in citrate buffer and exposure to high temperatur
e heating (100 degrees C) with a microwave. In our experience, the ben
efits of this technique as applied to cytoplasmic proteins does not ro
utinely translate to the nuclear estrogen and progesterone receptor (E
R and PgR) proteins. The lifting or loss of portions of a breast biops
y section can seriously interfere with efficient scoring of invasive t
umor cells. The use of low temperature restoration (80 degrees C) in c
itrate buffer using a water bath avoids problems of tissue disruption
and generally restores the immunoreactivity of ER and PgR proteins in
a more uniform fashion than does the microwave approach.