Figure 7.
Figure 7. Influence of NaCl concentration on the recognition of β2-GPI by anti-β2-GPI IgG antibodies. Plasma-purified β2-GPI and recombinant β2-GPI were coated to hydrophobic (A) and hydrophilic (B) plates. Subsequently, the plates were blocked with 4% BSA/TBS/Tween and incubated with (type A) patient plasma that was diluted in blocking solution with either 150 mM NaCl or 5 M NaCl. To detect the bound patient IgG antibodies, the plates were incubated with an alkaline-phosphatase-labeled goat anti-human IgG antibody. PnPP was used as coloring substance. Error bars represent mean ± SEM of quadruplicate points.

Influence of NaCl concentration on the recognition of β2-GPI by anti-β2-GPI IgG antibodies. Plasma-purified β2-GPI and recombinant β2-GPI were coated to hydrophobic (A) and hydrophilic (B) plates. Subsequently, the plates were blocked with 4% BSA/TBS/Tween and incubated with (type A) patient plasma that was diluted in blocking solution with either 150 mM NaCl or 5 M NaCl. To detect the bound patient IgG antibodies, the plates were incubated with an alkaline-phosphatase-labeled goat anti-human IgG antibody. PnPP was used as coloring substance. Error bars represent mean ± SEM of quadruplicate points.

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