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Series GSE38544 Query DataSets for GSE38544
Status Public on Jun 08, 2012
Title Gene expression signatures in anti-FGFR2IIIc monoclonal antibody-treated human colorectal cancer cells
Organism Homo sapiens
Experiment type Expression profiling by array
Summary To investigate the underlying mechanisms of the inhibitory effects of human anti-human FGFR2IIIc antibody on growth and migration of colorectal cancer cells, we used DNA microarray analysis to examine the cell signaling pathway alterations following the administration of anti-FGFR2IIIc antibody.
 
Overall design Cells were plated at a density of 2.5 × 105 cells in a 60-mm dish, and grown overnight. Then 100 μg/mL of monoclonal anti-human FGFR2IIIc antibody was added in each dish. For control groups, an equal amount of anti-GFP antibody was added in another dish. After 48 hr, total RNA was isolated from cells. For use in DNA microarray analysis, 50 ng RNA from each group of cells was labeled using the Low Input Quick Amp Labeling kit. Labeled RNA was further purified using the Qiagen RNeasy Mini kit. Labeled cRNA was hybridized to the Agilent human 44k oligonucleotide microarray, and washed using Agilent Gene Expression washing buffer.
 
Contributor(s) Matsuda Y, Ishiwata T
Citation(s) 22778155
Submission date Jun 07, 2012
Last update date Feb 22, 2018
Contact name Yoko Matsuda
E-mail(s) ymazda@nms.ac.jp
Organization name Nippon Medical School
Department Department of Pathology
Street address 1-1-5, Sendagi, Bunkyo-ku
City Tokyo
ZIP/Postal code 113-8602
Country Japan
 
Platforms (1)
GPL4133 Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Feature Number version)
Samples (4)
GSM945155 HCT-negative
GSM945156 HCT-FGFR Ab
GSM945157 LoVo-negative
Relations
BioProject PRJNA168215

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE38544_RAW.tar 42.2 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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