Rapid Communication
Copyright ©2008 The WJG Press and Baishideng.
World J Gastroenterol. Feb 7, 2008; 14(5): 758-763
Published online Feb 7, 2008. doi: 10.3748/wjg.14.758
Figure 1
Figure 1 In situ hybridization analysis of GCRG123 in gastric mucosa. GCRG123 showed low expression (blue precipitates restricted to the cytoplasm) in intestinal-type adenocarcinoma (A) and normal gastric glands (C, left region); high expression in signet-ring cell carcinoma (B); normal epithelia (C); and normal pyloric glands (D). NBT/BCIP was used as an alkaline phosphatase substrate (magnification was 10 × 10).
Figure 2
Figure 2 Northern blotting of GCRG123 in gastric tissues. The expression of β-actin served as an internal control. Total RNA, 1 &mgr;g per lane, was separated on a 1% agarose/formaldehyde gel. After blotting onto a nylon membrane, the membrane was probed with digoxigenin-labeled anti-sense GCRG123 cRNA. N, normal gastric tissue; T, tumor; 1, signet-ring cell carcinoma; 2, intestinal-type adenocarcinoma.
Figure 3
Figure 3 Multalin analysis of GCRG123 (AF454554) and L1 (HUMTNL22). Red font represents high consensus, blue or black font represents low consensus.