“…They concluded that wild-type p53 may be detectable in normal cells after using AR, and pointed out the importance of technical conditions as well as the evaluation of normal tissue controls in the clinical application of p53 immunostaining. Goulding et al (1995) performed a comparative study based on two MAbs to ER, 1D5 (Dako) and H222 (Abbott; N ); pH 6, 100C, 10 min ( E,O ); pH 6, 90C, 10 min ( F,P ); pH 10, 100C, 20 min ( G,Q ); pH 10, 100C, 10 min ( H,R ); pH 10, 90C, 10 min ( I,S ); no AR pretreatment ( J,T ). For MIB 1, the strongest intensity of staining was found in A, B, and G .…”