Release Date: 2017-01-18
Publication DOI: 10.15252/msb.20145644
License: CC BY 4.0
PubMed ID: 26148352
PMC ID: PMC4380925
High Content Analysis was used to quantitatively profile the morphology and NF-kappaB nuclear localization (which serves as a proxy for its activation), in 17 breast cancer and two non_tumor cell lines. Cells were treated with or without TNFa for 1 h or 5 h to capture the first peak and later steady state of NF-kappaB activation. Version History July 2017: screenA - updated some cell line names to be inline with the names used in EFO. MCF7 -> MCF-7, MCF10A -> MCF 10A, JIMT1 -> JIMT-1, MDA-MB-157 -> MDAMB157, MDA-MB-231 -> MDAMB231, MDA-MB-453 -> MDAMB453, SUM149 -> SUM149PT, SUM159 -> SUM159PT, ZR75.1 -> ZR751.
Sero JE, Sailem HZ, Ardy RC, Almuttaqi H, Zhang T, Bakal C
Data is available for download via Globus: idr0019-sero-nfkappab.
To download individual files in your browser, you can browse original data.
Download as JSON.
For more download options, including FTP, see the IDR Data download page.
Sample Type: cell
Organism: Homo sapiens
Study Type: high content analysis of cells
Screen Type:
Imaging Method: spinning disk confocal microscopy
Copyright: Sero et al
Annotation File: idr0019-screenA-annotation.csv
© 2016-2025 University of Dundee & Open Microscopy Environment. Creative Commons Attribution 4.0 International License.
OMERO is distributed under the terms of the GNU GPL. For more information, visit openmicroscopy.org