A Rapid Method forIn SituStaining of Prostatic and other Tissue Culture Cells

Abstract
A rapid method for staining prostatic epithelium grown in vitro and other tissue culture cells is described. Giemsa stain and a phosphate buffer with a pH of 6.8 were used. Excellent nuclearcytoplasmic contrast is obtained with this procedure. It is recommended for studies on the general morphology of normal and abnormal cells in tissue culture.