As a control we used the pEGFP-C1 vector producing GFP protein. Immunohistochemical

Analysis Tissue sections on microscopic slides were processed through a graded series of alcohols and rehydrated in distilled water. Heat-induced antigen retrieval was performed by hydrated autoclaving in citrate buffer (10 mmol/L concentration, pH 6.0) for 5 min. To minimize non-specific background reactivity, tissue sections were incubated with normal goat serum for 10 min. The slides were cooled to room temperature for 30 min to complete antigen unmasking, and standard indirect biotin-avidin immunohistochemical analysis was learn more performed to evaluate APMCF1 protein expression using a polyclonal anti-APMCF1 antibody (1:100 diluted) produced by our lab previously [3]. Incubation with non-immune rabbit serum and antibody blocked YH25448 with purified APMCF1 protein served as a negative control. Protein expression was scored by two observers as: absent (-); weakly positive (+), < 10% cells showed positive staining; moderately positive (++), 10–50% cells showed positive staining; or strongly positive (+++), > 50% cells

showed positive staining. Results Subcellular localization of APMCF1 protein For direct visualization of the cellular location of APMCF1, the corresponding cDNAs were cloned in frame with enhanced green fluorescent protein (EGFP) in the mammalian expression vector pEGFP-C1, followed by transient transfection into green monkey kidney epithelial cells (COS-7). Typical patterns are shown in Figure 1. In singly transfected cells, fluorescence was dispersed throughout the cytoplasm. Figure 1 Subcellular localization of the EGFP-APMCF1 fusion protein. COS-7 cells were transfected with pEGFP-C1-APMCF1 or pEGFP-C1 vector. Twenty-four hours after transfection, subcellular localization Cyclooxygenase (COX) of EGFP-APMCF1 fusion proteins was examined by direct fluorescent microscopy. (A) green fluorescence

was seen in the cell cytoplasm of COS-7 cells transfected with pEGFP-C1-APMCF1; (B) green fluorescence was seen in the cell nuclei and cytoplasm of COS-7 cells transfected with pEGFP-C1. Expression of APMCF1 in normal and malignant human tissues Brown labeling represented the presence of APMCF1. The relative intensity was scored from (-) to (+++). Specific cytoplasmic staining was MK-4827 observed in the majority of positive stained cells, suggesting that APMCF1 was a cytoplasmic protein. Generally, APMCF1 was detected in the parenchymal cells of liver, lung, breast, colon, stomach, esophagus and testis, including the malignant tumor, tumor-adjacent tissues and normal tissues. Normal brain neuron cells also showed expression of APMCF1, but no detectable labeling was observed in brain gliocyte cells and glioma. Both the normal and tumor tissues of ovary were absent of APMCF1 expression. Representative photomicrographs are presented in Figure 2.