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. 2017 Jul 1;13:644–649. doi: 10.1016/j.dib.2017.06.048
Subject area Biology
More specific subject area Liver biology
Type of data Figures (Immunofluorescence staining, Western blot analysis)
How data was acquired Microscope (Nikon ECLIPSE 80i)
Chemiluminescent detection (Boehringer Mannheim GmbH Lumi-Imager)
Data format Raw
Experimental factors Liver sections were derived from WT and Lcn2-/-mice[2]after feeding a MCD or standard chow diet for 6 weeks.
Protein extracts were prepared from the same livers for Western blot analysis.
Hepatocytes were isolated from WT and Lcn2-/-mice for in vitro experimentation.
Experimental features Liver sections from WT and Lcn2-/-mice were immunostained for PIP3. Negative and positive controls were also used.
100 µg of protein extracts from livers were used to detect PKB, phospho PKB, LCN2 and Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) by Western blot.
Hepatocytes were cultured from WT and Lcn2-/-mice. These were left untreated or treated with bovine insulin to induce PI3K and PIP3. Respective cells were immunostained for PIP3.
Data source location Aachen, Germany
Data accessibility Data not deposited elsewhere outside this article. Primary data are published in[1].