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. 2009 Oct 30;2(6):1384–1396. doi: 10.1093/mp/ssp085

Figure 2.

Figure 2.

Detection of PRK in Elysia chlorotica.

(A) PRK Western blot using a tobacco PRK antibody and the alkaline phosphatase detection system. Extracts were loaded on an equal chlorophyll basis as follows: E-kp, E. chlorotica kleptoplasts (from animals starved nine months); V-cp, V. litorea plastids; S-cp, spinach plastids; E-tp, E. chlorotica total proteins (from animals starved for 3 months); V-tp, V. litorea total proteins.

(B) Western blot and fluorogram of immunoprecipitated PRK from 5-month-starved sea slugs, following labeling with [35S]methionine/cysteine for 6 h and separation by SDS–PAGE.