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. 2017 May 5;24(6):1029–1044. doi: 10.1038/cdd.2017.32

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Copyright © 2017 The Author(s)

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/

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SLY protein interacts with TBL1XR1 protein. (a) SLY and TBL1XR1 antibody detection of WT and Sly-deficient (Sly-KD) whole-testicular extracts (INPUT) and of corresponding extracts immunoprecipitated with SLY antibody (IP:SLY). SLY immunoprecipitation performed on Sly-KD testicular extracts and immunoprecipitation with purified rabbit IgG on WT extracts (IP:IgG) were used as negative controls. (b) SLY and TBL1XR1 antibody detection of whole-testicular extracts from WT and FLAG-SLY mice (INPUT) and of corresponding extracts immunoprecipitated with FLAG antibody (IP:FLAG). FLAG immunoprecipitation performed on WT testicular extracts was used as a negative control. (c) SLY and TBL1XR1 antibody detection of WT whole-testicular extracts (INPUT) and immunoprecipitated with TBL1XR1 antibody (IP:TBL1XR1). TBL1XR1 immunoprecipitation performed on Sly-KD testicular extracts and immunoprecipitation with purified rabbit IgG on WT extracts (IP:IgG) were used as negative controls. Arrows indicate the specific band (at expected sizes of 38kDa for SLY and 64kDa for TBL1XR1) and stars, non-specific bands (which disappear in negative controls)