Skip to main content
. 2016 Dec 9;10:449–453. doi: 10.1016/j.dib.2016.12.001
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.