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. 2015 Apr 9;9(4):e0003617. doi: 10.1371/journal.pntd.0003617

Fig 1. Immunoblotting to evaluate antibody binding to B. turicatae protein lysates, rGlpQ, and rBipA (A).

Fig 1

The asterisk and arrowhead represent the molecular masses for native GlpQ and BipA, respectively (A). rBipA was produced as a thioredoxin fusion protein and is 15 kDa larger than the native protein. Immunoblots were also probed with a serum sample from an uninfected patient (B) and a monoclonal antibody against the six-histidine fusion tag (C and D). Molecular masses are shown to the left of each immunoblot.