Abstract
Either citric acid or ascorbic acid (0.23 m final concentration) quickly arrests incorporation of tritiated thymidine or uridine upon addition to cultures of animal cells. The incorporated radioactivity is totally preserved for a day at 37°C without further manipulations. In contrast, radioactivity is extensively lost from cultured cells at 37°C after they are arrested by the conventional method of trichloroacetic acid precipitation following removal of medium and rinsing. The cells arrested with citric or ascorbic acid preserve their morphology and are suitable for autoradiography. The new method has considerable advantages of convenience and accuracy over treatment with trichloroacetic acid.
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