NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM803673 Query DataSets for GSM803673
Status Public on Sep 29, 2011
Title BR:T47D [113442hp133a11]
Sample type RNA
 
Source name infiltrating ductal carcinoma
Organism Homo sapiens
Characteristics tissue of origin: Breast
cell line: T47D
age: 54
Sex: F
epithelial: yes
ploidy: 2n+, Hyperdiploid (47-57)
p53 mutation: MT
doubling time: 45.5
contributing person: I. Keydar
reference: Eur J Cancer 15:659-679,1979
Treatment protocol No treatment
Growth protocol Cells grown in RPMI 1640 with 5% FBS (Bio Whittaker, not heat inactivated) and 1% L-glutamine. Cells not grown past 80% confluencey for attached cells, or 0,5 x 10-6 cells for suspended. Trypsinize (for attached cells) cells with 5 ml trypsin-EDTA per T162, for 15 min., at 370C. Spin down suspended cells, and resuspend in ~3ml growth media. Count cells. Pass 1x10-6 cells into new T162’s w 30 ml media. Repeat growth cycle until desired amount of cells are available. Cells are not grown past passage 20.
Extracted molecule total RNA
Extraction protocol Growth schedule prior to harvest: Grow cells to ~80 confluencey. Re-feed cells the day prior to harvest. Draw off media from attached cells, or spin down suspended cells. Rinse cells with ~10 ml 1x PBS. Purify using Quiagen Midi Kit (Cat # 75144) per instructions. In brief, lyse cells in 15 ml lysis buffer (w 10 ul fresh BME per ml) per 4 T162s. Scrape (attached) cells. Pipet into a 50 ml tube. Repeat with the next set of 4 flasks. When done, vortex 10 sec.. Draw lysate thru a 20 guage needle 12x’s. Freeze lysate at -80 deg C. Use a maximum of 100 x 10-6 cells per column.
Label biotin
Label protocol Done by Genelogic according to manufacturer's recommendations
 
Hybridization protocol Done by Genelogic according to manufacturer's recommendations
Scan protocol Affymetrix MicroArraySuite
Description infiltrating ductal carcinoma
Data processing Probes were normalized using RMA in Partek Genomics Suite version 6.2
 
Submission date Sep 29, 2011
Last update date Sep 29, 2011
Contact name Sudhir Varma
E-mail(s) sudhirv4rma@gmail.com
Organization name HiThru Analytics
Street address 1215 Wessex Pl
City Princeton
State/province NJ
ZIP/Postal code 08540
Country USA
 
Platform ID GPL570
Series (1)
GSE32474 Comparison between cell lines from 9 different cancer tissue (NCI-60) (Affymetrix U133 Plus 2.0)

Data table header descriptions
ID_REF
VALUE Probeset expression is in log2 units

Data table
ID_REF VALUE
1007_s_at 10.79903793
1053_at 7.821648121
117_at 5.013325214
121_at 7.294297218
1255_g_at 2.746088982
1294_at 5.602688789
1316_at 5.061889172
1320_at 6.080884933
1405_i_at 2.821448088
1431_at 3.280859947
1438_at 6.81492281
1487_at 7.708965778
1494_f_at 4.994367123
1552256_a_at 8.586953163
1552257_a_at 7.484737873
1552258_at 4.138133049
1552261_at 4.078900814
1552263_at 4.682627201
1552264_a_at 7.320436001
1552266_at 2.838980913

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM803673_113442hp133a11.cel.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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