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. 2005 Mar;12(3):380–386. doi: 10.1128/CDLI.12.3.380-386.2005

FIG. 1.

FIG. 1.

(A) Structure of camelid IgGs (data from reference 12). (B, top) Coomassie blue-stained SDS-PAGE gel of purified llama IgG isotypes resolved under nonreducing and reducing conditions. (a and b) IgG1 and IgG3 (eluted from protein G); (c) IgG2 (eluted from protein A). (Bottom) Western blot of gels identical to Coomassie blue-stained gels developed with polyclonal anti-llama IgG (H+L). Molecular masses (in kilodaltons) of protein standards run in parallel are indicated.