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. Author manuscript; available in PMC: 2015 Mar 1.
Published in final edited form as: FEBS J. 2014 Feb 13;281(6):1571–1584. doi: 10.1111/febs.12724

Figure 5. SLX/SLXL1 proteins are not visible in the nucleus of MSYq− spermatids.

Figure 5

(A) Detection of SLX/SLXL1 proteins (green) by immunofluorescence in WT, shSLY and MSYq− testis sections. DAPI (blue) was used to stain nuclei and lectin-PNA (red) was used to stain acrosomes. The inset in the upper left corner represents a 2.5 magnification. Scale bar indicates 10μm. (B) Representative pictures of the detection of SLX/SLXL1 proteins (green) by immunofluorescence in WT, shSLY and MSYq− round spermatid nuclei (surface spread technique). DAPI (grey or blue) was used to stain nuclei. No signal can be detected in MSYq− round spermatid nuclei.