Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 May 13;9(5):49. doi: 10.1038/s41389-020-0236-x

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Fig. 2 — a Flow cytometry analysis of apoptosis in LNCaP cells with increasing doses of Carbidopa. b TUNEL assay in LNCaP cells. Cells were treated with increasing doses of Carbidopa; apoptotic cells were labeled green, and nuclei blue (DAPI). Figure shows merged images. Scale bars = 100 μm. c Quantitative analysis of TUNEL+ cells in at least six separate fields; data are given as means ± SEM. *p < 0.05 versus control. **p < 0.01 versus control. d Cell lysates of LNCaP cells were used to detect the Bax, Bcl-2, and cleaved caspase-3 protein levels by immunoblotting. e Quantitative analysis of each immunoblot; results were normalized to control and data are given as means ± SEM. *p < 0.05 versus control.