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. 2010 Jun 10;5(6):e11047. doi: 10.1371/journal.pone.0011047

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This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.

This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.

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Plates were coated with the capture antibody: F24-1 ♦; F26-16 ■; F27-33 ▲; F29-40 □; MCS6-27 ●. A. pH of capture buffer (1×TBS) was adjusted for each capture antibody at concentrations of SDS as follows; F24-1, 0.7 mM; F26-16, 0.5 mM; F27-33, 0.6 mM; F29-40, 0.6 mM; MCS6-27, 0.3 mM. B. Concentration of SDS in capture buffer was adjusted for each capture antibody at the following pH; F24-1, pH 6.0; F26-16, pH 7.5; F27-33, pH 6.0; F29-40, pH 8.0; MCS6-27, pH 8.0. Data are presented as average of 3 samples ±1 standard error.