NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM543398 Query DataSets for GSM543398
Status Public on Dec 31, 2010
Title MB231 transfected with AllStar, biological rep2
Sample type RNA
 
Source name MDA-MB-231 cells grown in 6 well dishes 48 hrs post-transfection
Organism Homo sapiens
Characteristics cell line: MDA-MB-231
Treatment protocol MDA-MB-231 cells (600,000 cells/well) were reverse transfected in 6 well dishes with either AllStar negative control, Qmimic, or Dmimic at 10 nM final concentration using Lipofectamine 2000 (10.5 ul/well),
Growth protocol MDA-MB-231 cells were grown in T75 flasks containing RPMI 1640 basal medium + 10% Fetal Bovine Serum at 37C with 5% CO2. Cells at 80-90% confluency were used in transfections.
Extracted molecule total RNA
Extraction protocol At 48 hrs post-transfection, total RNA was extracted from each well using Qiagen's miRNeasy extraction kit according to the manufacturer's instructions.
Label biotin
Label protocol RNA quality ws assessed on an Agilent Bioanalyzer. Total RNA (1 ug) was reverse transcribed with T7-oligo(dT) primer and labeled with biotin using Affymetrix One Cycle Target Labeling kit following the manufacturer's protocol.
 
Hybridization protocol cRNA was hybridized for 16 hrs at 45C (60 rpm). GeneChips were washed and stained in the Affymetrix FS450 fluidics station.
Scan protocol GeneChips were scanned using a Affymetrix GeneChip 3000 Scanner. Data was collected using Affymetrix GCOS software.
Description Gene expression data of total RNA extracted from MB231 cells 48hrs post-transfection
Data processing Expression values were normalized using Robust Multichip Averaging (RMA). Analyses were performed with Bioconductor packages AFFYGUI and LIMMA on a R environment.
 
Submission date May 14, 2010
Last update date Dec 31, 2010
Contact name Mark Mackiewicz
E-mail(s) mackiewiczm@mail.nih.gov
Phone 301-594-6044
Fax 301-480-8878
Organization name National Institutes of Health
Department National Cancer Institute
Lab Genetics Branch
Street address 37 Convent Drive
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL570
Series (2)
GSE21832 Identification of the receptor tyrosine kinase AXL in triple negative breast cancer as a novel target for the human miR-34a microRNA (gene expression)
GSE21834 Identification of the receptor tyrosine kinase AXL in triple negative breast cancer as a novel target for the human miR-34a microRNA

Data table header descriptions
ID_REF
VALUE Robust Multichip Averaging (RMA) signal intensity

Data table
ID_REF VALUE
117_at 5.240191449
121_at 8.153415399
177_at 5.472003115
179_at 8.707613287
243_g_at 10.22176271
266_s_at 3.836663515
320_at 7.775710903
336_at 6.637982948
396_f_at 8.593609053
564_at 9.59330166
632_at 7.430005523
635_s_at 7.120594557
823_at 5.162476986
1007_s_at 9.559180401
1053_at 9.027820282
1255_g_at 3.395178921
1294_at 7.203601957
1316_at 5.820402518
1320_at 6.603025118
1405_i_at 3.500628184

Total number of rows: 54675

Table truncated, full table size 1211 Kbytes.




Supplementary file Size Download File type/resource
GSM543398.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap