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. 2008 Oct 24;19(2):126–134. doi: 10.1093/glycob/cwn110

Fig. 5.

Fig. 5

Binding activity of N162-shFcγRIIIa-His to IgG1. The purified N162-shFcγRIIIa-His was loaded onto a column of nonfucosylated IgG1-immobilized Sepharose. The fractions of load (lane 1), flowthrough (lane 2), and elution (lane 3) were subjected to nonreducing (A) and reducing (B) 5–20% SDS–PAGE. No detectable protein was observed in the flowthrough fraction, and the whole flowthrough fraction was concentrated to apply SDS–PAGE.