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. 2018 Apr 2;200(9):3053–3066. doi: 10.4049/jimmunol.1701673

FIGURE 1.

FIGURE 1.

(A) Binding titration of mAbs to purified LAMs isolated from M. tuberculosis (ManLAM), M. leprae (LepLAM), and M. smegmatis (PILAM). After coating the Ags (20 μg/ml) on ELISA plates, the plates were blocked by incubation with a solution of 1% BSA and titered against a panel of 10 mAbs reactive with LAM carbohydrate structures. Ab binding was detected with the appropriate AP-labeled secondary Ab. (B) Tabulation of the 50% maximum binding concentration (μg/ml) of each mAb for each of the Ags. Nonreactive combinations are highlighted in yellow.