Receptor-mediated gene transfection1 has gained central interests since Wu and Wu2 demonstrated successful gene transfection into hepatocytes by using an asialoglycoprotein-poly(L-lysine) complex as a nonviral gene vector. Besides the hepatoma cells possessing galactose-specific receptor proteins, macrophages bearing mannose-specific receptors can also become a target of the gene transfection.3-5 Though partially mannosylated poly(L-lysine)3,4 and mannosylated avidin5 have been tested for this purpose, development of more effective vectors with higher cytoselectivity is required for gene therapies. As a part of our research efforts to develop and apply artificial glycoconjugate polymers carrying biologically active oligosaccharides,6-8 our interest has been directed to the potential utility of 3,6-branched α-D-mannoside for the receptor mediated gene transfer targeting macrophages. The 3,6-branched mannosyl trisaccharide is reported to be the much better ligand of mannose-specific binding proteins than mono- and linear oligomannosides.9 In this communication, we report a facile synthesis of a glycoconjugate cationic polymer carrying the 3,6-branched α-D-mannoside cluster10,11 and evaluate its binding affinity to a mannose-specific lectin, concanavalin A.