NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM803706 Query DataSets for GSM803706
Status Public on Sep 29, 2011
Title RE:UO_31 [113475hp133a11]
Sample type RNA
 
Source name Renal cell carcinoma
Organism Homo sapiens
Characteristics tissue of origin: Renal
cell line: UO_31
Sex: F
prior treatment: None
epithelial: yes
ploidy: 2n+/-, Near-diploid 46+/- (35-57)
p53 mutation: WT
doubling time: 41.7
contributing institute: National Cancer Institute, NIH
contributing person: W.M.Linehan
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 Renal cell carcinoma-very poorly differentiated
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 10.08993721
1053_at 7.342600822
117_at 4.653004169
121_at 9.758467674
1255_g_at 2.715498924
1294_at 7.396877766
1316_at 5.148087025
1320_at 5.215312958
1405_i_at 2.878968
1431_at 3.13547802
1438_at 5.104255199
1487_at 7.751976967
1494_f_at 5.048997879
1552256_a_at 7.556480885
1552257_a_at 7.730768204
1552258_at 4.405527115
1552261_at 4.317520142
1552263_at 4.647478104
1552264_a_at 7.415627003
1552266_at 2.903652906

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM803706_113475hp133a11.cel.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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