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. Author manuscript; available in PMC: 2008 Oct 7.
Published in final edited form as: J Cell Biochem. 2008 Aug 1;104(5):1843–1852. doi: 10.1002/jcb.21752

Fig. 3. Knockdown of ceMTM3 expression by RNAi.

Fig. 3

Normal N2 worms were fed with E. coli cells carrying vector control, full-length ceMTM3b, and two ceMTM3b cDNA fragments (ceMTM3bF1 and ceMTM3bF2) as indicated in A. B. Crude cell extracts containing equal amounts of total proteins were subjected to Western blotting analyses. C. Paraffin-embedded worm sections were stained with anti-ceMTM3 antibody. D. The phosphatase activity of immunoprecipitated ceMTM3 was determined with 5 μM PI3P substrate at pH 6.0 as described in Fig. 2A. Error bars denote standard deviation (n = 4).