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. 2015 Aug 21;2(4):135–138. doi: 10.5152/eurjrheum.2015.0012

Figure 3.

Figure 3

a–d. Tests standards (high, medium, and low) were tested on each IgA anti-β2 GPI assay, and anti-human IgA conjugates were interchanged (blue from assay A and red from assay B).

There was a 4 times stronger reactivity of conjugate A when tested on assay B than conjugate B, suggesting that IgA detection in assay B is partially dependent on the IgA conjugate and calibration.

Standards A on assay A (a), standards B on assay B (b), standards A on assay B (c), standards B on assay B (d), and conjugate B did not elicit IgA anti-β2 GPI antibody reactivity when tested on assay A (a–c) but only when tested on assay B (d)