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. 2010 Oct 27;41(1):214–223. doi: 10.1002/eji.201040612

Figure 2.

Figure 2

Oligomeric structure of rat ficolin-B. (A) Purified ficolin-B separated by SDS-PAGE (4–12% gradient gel) under reducing and non-reducing conditions. Proteins were stained using Coomassie blue. (B) Gel filtration of ficolin-B on a Superdex-200 column. The elution positions of monomers (M), dimers (D), trimers (T) and tetramers (Tt) of rat ficolin-B are indicated. (C) Fractions collected across the gel filtration peaks were separated by gel electrophoresis on a 4–12% gradient SDS-polyacrylamide gel under non-reducing conditions, and proteins were stained with Coomassie blue.