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. 2012 Jun 1;13(8):671–680. doi: 10.4161/cbt.20084

graphic file with name cbt-13-671-g1.jpg

Figure 1. Expression of CXCL4 in normal, endometriosis and cancer tissues. (A) western blot analysis is performed using anti-CXCL4 antibody that recognizes both CXCL4 and CXCL4-L1. Representative cases of normal, endometriosis and cancer tissues are shown. β-actin is used as a control. Platelet-derived protein is used as positive control. (B) Results of RT-PCR analysis are shown. CXCL4-specific and CXCL4-L1-specific primers are used, respectively. The PCR product samples were subjected to 2% agarose gel electrophoresis and visualized by staining with ethidium bromide. (C) Real-time RT-PCR was performed and the expression levels of CXCL4 (left graph) and CXCL4-L1 (right graph) normalized by GAPDH were investigated among normal (n = 26), endometriosis (n = 18), clear cell cancer (n = 13) and endometrioid cancer (n = 11) tissues.