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Status |
Public on Dec 26, 2018 |
Title |
MCF-10A + Crb3 rep2 |
Sample type |
RNA |
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Source name |
MCF-10A human mammary epithelial cell line
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Organism |
Homo sapiens |
Characteristics |
treatment: retroviral overexpression of Crb3 culture condition: Cells were cultured in normal MCF-10 growth media. RNA was harvested from proliferating monolayers at 70% confluence. cell line: MCF-10
|
Treatment protocol |
MCF-10A cells were retrovirally infected with Crb3 or vector control and puromycin selected.
|
Growth protocol |
Cells were cultured in normal MCF-10 growth media.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated according to manufacturer’s protocol with TRIzol-reagent (Invitrogen).
|
Label |
biotin
|
Label protocol |
Biotinylated cRNAs were prepared according to the Affymetrix standard labeling protocol.
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Hybridization protocol |
Following fragmentation, cRNAs were hybridized to the Affymetrix GeneChip Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
|
Scan protocol |
GeneArray Chip Scanner, HP/Affymetrix Inc.
|
Data processing |
Background correction and normalization was performed using the Robust Multichip Average method implemented in the rma function of R/BioConductor. Differential expression was assessed using the empirical Bayes method implemented in the limma package. The criteria for selecting differentially expressed genes was a false discovery rate (FDR)-corrected p-value of less than 0.05 and a fold change greater than 1.5.
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Submission date |
Jan 06, 2016 |
Last update date |
Dec 26, 2018 |
Contact name |
Joan S. Brugge |
E-mail(s) |
joan_brugge@hms.harvard.edu
|
Organization name |
Harvard Medical School
|
Department |
Department of Cell Biology
|
Lab |
Brugge
|
Street address |
240 Longwood Avenue
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE76610 |
Overexpression of Crumbs3/CRB3 in human mammary epithelial line MCF-10A |
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