| Subject area | Biology |
| More specific subject area | 2-deoxy-d-glucose treatment, O-GlcNAcylation of cellular proteins |
| Type of data | Western blotting |
| How data was acquired | Western blotting using a chemiluminescent substrate (ECL Prime Western Blotting Detection Reagent, GE Healthcare UK Ltd.) and an image analyzer (Light-Capture ATTO Co.). |
| Data format | Raw data for Western blotting |
| Experimental factors | Cells were treated with 2-deoxy-d-glucose (2DG) and cellular proteins were analyzed by ECL Prime Western Blotting system. |
| Experimental features | Human teratocarcinoma NCCIT cells were incubated with a culture medium supplemented with 10 mM 2DG for 24–168 h. Protein extracts of the cells and the immunoprecipitates of anti-Sp1 antibody (D4C3) were subjected to Western blotting. |
| Data source location | Bioproduction research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 6, Tsukuba |
| Data accessibility | The data are provided in this article. |