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Sample GSM803684 Query DataSets for GSM803684
Status Public on Sep 29, 2011
Title BR:MDA_MB_231 [113453hp133a11]
Sample type RNA
 
Source name Adenocarcinoma-mammary gland; breast; epithelial; metastatic site: pleural effusion;
Organism Homo sapiens
Characteristics tissue of origin: Breast
cell line: MDA_MB_231
age: 51
Sex: F
epithelial: yes
source: Pleural effusion
ploidy: 2n+, Hyperdiploid (47-57)
p53 mutation: MT
doubling time: 41.9
contributing institute: MD Anderson Hospital and Tumor Institute
contributing person: R. Cailleau
reference: JNCI 53(3): 661-674,1974
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 Adenocarcinoma-mammary gland; breast; epithelial; metastatic site: pleural effusion;
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 9.17508316
1053_at 8.525650978
117_at 4.800499916
121_at 7.80053091
1255_g_at 2.71085
1294_at 6.800013065
1316_at 5.053475857
1320_at 5.584406853
1405_i_at 2.869541883
1431_at 3.112659931
1438_at 5.738721848
1487_at 7.957274914
1494_f_at 5.249248028
1552256_a_at 7.530086994
1552257_a_at 7.96097517
1552258_at 5.08042717
1552261_at 4.367607117
1552263_at 5.406269073
1552264_a_at 7.781342983
1552266_at 2.628910065

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM803684_113453hp133a11.cel.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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