Skip to main content
. 2011 Aug 25;22(3):379–388. doi: 10.1093/glycob/cwr110

Fig. 3.

Fig. 3.

Schematic representation of the expression constructs (A) pLgals1-hum-β3GN-T2 and (B) pLgals1-hum-MFng. The PCR-amplified DNA sequences were inserted in the pLgals1-Tev vector construct at the multicloning site, which is preceded by the 6HisTag and Tev cleavage site.