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. Author manuscript; available in PMC: 2016 Feb 25.
Published in final edited form as: Int J Parasitol. 2008 Nov 27;39(6):683–692. doi: 10.1016/j.ijpara.2008.11.002

Fig. 5.

Fig. 5

Reactivity of rPfRON6-A, -B and -C recombinant proteins with human immune sera. rPfRON6-A and -B were expressed and purified as GST fusion proteins. rPfRON6-C was expressed and purified as a hexa-histidine fusion. rPfRON6-A (lane 2), -B (lane 3), -C (lane 4) and a GST (lane 1) control were resolved by SDS-PAGE, and either stained with coomassie (loading control) or transferred to PVDF membrane and immunoblotted with human sera from individuals living in malaria endemic areas of Papua New Guinea (PNG) and Vietnam or with sera from naïve individuals living in Melbourne, Australia.