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. 2016 Apr 28;11(4):e0154101. doi: 10.1371/journal.pone.0154101

Fig 2. Analysis of the expression levels of the MIL-translocation machinery in different Leishmania strains.

Fig 2

Extracts from (A) L. infantum LEM3323 (3323), LEM3323-MIL (3323MIL), LiMT-transfected LEM3323-MIL (LEM3323-MIL + LiMT), (B) LEM3049, LEM5159, LiRos3- and LiMT-transfected LEM5159 (LEM5159 + LiRos3; 5159 + LiMT), (C) L. donovani ΔLdMT promastigotes transfected with LiMT GFP and with LiMTE926QGFP and (D) ΔLiRos3 and ΔLiRos3 + LiRos3 lines were subjected to SDS/PAGE and immunoblotted with the rabbit polyclonal anti-LdMT and anti-LdRos3 antibodies. Anti-α-tubulin monoclonal antibody was used as a probe for a protein loading control.