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. 2016 Jan 25;11(1):e0147559. doi: 10.1371/journal.pone.0147559

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© 2016 Nguyen et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 3 — Chicken sperm lysates (45μg of protein) were analyzed by western blotting using anti- CaMKI as primary antibody. Cell lysates from chicken muscle (40μg of protein) were used as positive control. A band of approximately 41kDa for CaMKI was detected (3A). Indirect immunofluorescence of chicken sperm was carried out with the same antibody. Negative control: primary antibody was not added (3B). White arrows and circles in transmission images indicate areas of the acrosome (arrow 1), the nuclei (arrow 2), the midpiece (circles), and the principal piece of the flagellum (arrow 3) in sperm (3C). Immunofluorescence staining of CaMKI (3D, green) was conducted; nuclei were stained with DAPI (3E, blue). Merged images of fluorescence with DAPI staining are shown in Fig 3F (white arrows indicate regions containing CaMKI immunoreactivity: arrow 1: acrosome; arrow 3: principle piece; circle: midpiece). Scale bar: 10μm.