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. Author manuscript; available in PMC: 2016 Nov 11.
Published in final edited form as: J Cell Sci. 2008 May 13;121(11):1937–1949. doi: 10.1242/jcs.023150

Fig. 4.

Fig. 4

Parasite actin distribution in the erythrocytic cycle. (A) Western blot of 15 μg of erythrocyte (E) or parasite (P) protein showing the anti-actin antibody is specific for parasite actin and non-reactive with erythrocyte actin. (B) Pfactin in the triton-soluble (gray) and triton-insoluble (black) fractions was quantified by densitometric analysis of western blots using a parasite specific anti-actin antibody in ring (n=4), trophozoite (n=6) and schizont (n=5) stage PE. (C) Triton-soluble (gray) and triton-insoluble (black) Pfactin fractions were separated from trophozoites following JAS (n=6) or CD (n=6) treatment, and quantified by densitometric analysis of western blots using a parasite specific anti-actin antibody. Data are expressed as a percentage of total Pfactin±s.e.m.