Archive image from page 148 of Cytochemistry a critical approach (1953). Cytochemistry: a critical approach cytochemistrycri00dani Year: 1953 Plate IV. Rat-kidney tubule sections (fixative 80 percent alcohol), dem- onstrating the Gomori-Takamatsu technique for alkaline phosphatase. Figure A, incubated 20 minutes. Compare this figure with Plate III, Fig. B. By comparison the nuclei of the alcohol-fixed section are grossly precipi- tated, and during fixation phosphatase has diffused from the cell borders into the cytoplasm. Figure B, incubated 5 minutes: the main sites of phosphatase are alrea


Archive image from page 148 of Cytochemistry a critical approach (1953). Cytochemistry: a critical approach cytochemistrycri00dani Year: 1953 Plate IV. Rat-kidney tubule sections (fixative 80 percent alcohol), dem- onstrating the Gomori-Takamatsu technique for alkaline phosphatase. Figure A, incubated 20 minutes. Compare this figure with Plate III, Fig. B. By comparison the nuclei of the alcohol-fixed section are grossly precipi- tated, and during fixation phosphatase has diffused from the cell borders into the cytoplasm. Figure B, incubated 5 minutes: the main sites of phosphatase are already apparent. Figure C is a section containing phos- phatase superimposed on a section in which phosphatase has been destroyed. Incubation time, 320 minutes. The active section has been grossly over- incubated and appears almost opaque. The microscope was focussed on the underlying section, which is devoid of phosphatase activity, but which shows a faint image by diffraction. The absence of any apparent phos- phatase activity in the underlying section shows that, during the incubation period of 320 minutes, no significant amount of phosphatase or of calcium phosphate has diffused into the underlying section, so that there is clearly no significant diffusion artefact. Figure D is the same as Fig. C, but incu- bated 640 minutes. By this time some of the nuclei of the underlying inert section appear black, showing that either calcium phosphate or phos- phatase has diffused into the underlying section. The intensity of staining of the nuclei of the inert section has been deliberately exaggerated in the photograph to provide contrast with the unstained background seen by diffraction.


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