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    Figure 1.

    Indirect immunofluorescence assay detection of Borrelia crocidurae Achema strain (A and B; magnification: ×400) and clinical isolate B. crocidurae 03–02 (C and D; magnification: ×600) by purified mouse monoclonal antibodies (MAbs): P3A10 (A and C at 1:500 and 1:1,000 dilution, respectively) and P6D9 (B and D at 1:500 and 1:1,000 dilution, respectively). Monoclonal antibodies were tagged using a goat anti-mouse IgG conjugated to fluorescein isothiocyanate at 1:400 dilution. These two mentioned MAbs are available for research purposes upon request from the corresponding author.

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The authors of an article previously published by the AJTMH (Monoclonal Antibodies for the Diagnosis of Borrelia crocidurae by Fotso Fotso and others (https://www.ajtmh.org/content/journals/10.4269/ajtmh.15-0436) draw attention to errors in Figure 1 of that article. These resulted from errors by a researcher that were missed by other authors. Specifically, a single image was inappropriately inserted to represent three different experiments. A corrected Figure 1 is shown below.

Figure 1.
Figure 1.

Indirect immunofluorescence assay detection of Borrelia crocidurae Achema strain (A and B; magnification: ×400) and clinical isolate B. crocidurae 03–02 (C and D; magnification: ×600) by purified mouse monoclonal antibodies (MAbs): P3A10 (A and C at 1:500 and 1:1,000 dilution, respectively) and P6D9 (B and D at 1:500 and 1:1,000 dilution, respectively). Monoclonal antibodies were tagged using a goat anti-mouse IgG conjugated to fluorescein isothiocyanate at 1:400 dilution. These two mentioned MAbs are available for research purposes upon request from the corresponding author.

Citation: The American Journal of Tropical Medicine and Hygiene 103, 2; 10.4269/ajtmh.15-0436err

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