Journal of Andrology Proceedings of the Fifth International Conference on the Epididymis
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Right arrow Help viewing high resolution images
Right arrow Return to article

Figure 7


Figure 7. (A) Reverse transcription polymerase chain reaction analysis of caspase-3 mRNA expression in Leydig cells cultured for 24 hours in control medium (C) and medium supplemented with hepatocyte growth factor (HGF). (B) Western blot analysis of proteins extracted from control and HGF-treated Leydig cells. Proteins were detected with an anti–caspase-3 polyclonal antibody and anti-tubulin monoclonal antibody. (C) Densitometric scanning of the active fragment (17 kd) of caspase-3. The values of the samples treated with HGF are reported as percentages with respect to the control values arbitrarily considered as "1." (D) Values of the densitometric scanning of caspase-3 active fragment (dark columns) and precursor (dotted columns) in control and HGF-treated cells. In C and D, the X ± SE of the 3 experiments performed is reported and (*) vs C, P < .05.





Right arrow Return to article


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS