Phosphomannose isomerase(PMI)encoding gene manA is a desirable selective marker in transgenic research.Understanding of its expression patterns in transgenic plant and establishing highly sensitive detection method based on immunoassay have great impacts on the application of PMI.In this study,PMI-specific monoclonal antibodies were generated using recombinant protein as immunogen,and could be used in Western blot to detect as little as 0.5 ng His-tagged PMI protein or rice expressed PMI protein in sample accounted for 0.4%of single rice grain(about 0.08 mg).PMI protein driven by CaMV-35S promoter was detected in dozens of tested tissues,including root,stem,leaf,panicle,and seed at all developmental stages during rice growing,and PMI protein accounted for about 0.036%of total protein in the leaves at seedling stage.The established method potentially can be used to monitor PMI protein in rice grains. Phosphomannose isomerase (PMI) encoding gene manA is a desirable selective marker in transgenic research. Understanding the expression patterns of in transgenic plants and establishing highly sensitive detection method based on immunoassay have great impacts on the application of PMI. In this study, PMI-specific monoclonal antibodies were generated using recombinant protein as immunogen, and could be used in Western blot to detect as little as 0.5 ng His-tagged PMI protein or rice expressed PMI protein in sample accounted for 0.4% of single rice grain (about 0.08 mg). PMI protein driven by CaMV-35S promoter was detected in dozens of tested tissues, including root, stem, leaf, panicle, and seed at all developmental stages during rice growing, and PMI protein accounted for about 0.036% of total protein in the leaves at seedling stage. The established method potentially can be used to monitor PMI protein in rice grains.