NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM416671 Query DataSets for GSM416671
Status Public on Jan 28, 2010
Title NOSE cell culture, biological rep3
Sample type RNA
 
Source name Normal ovarian surface epithelium (NOSE) cell culture
Organism Homo sapiens
Characteristics cell line: Normal ovarian surface epithelial (NOSE) cells
Growth protocol Primary cultures of normal ovarian surface epithelium (NOSE) were performed as previously described. Briefly, brushings of the ovarian surface were performed in pre- and postmenopausal women undergoing clinically indicated surgery. NOSE cells were cultured in 1:1 MCDB105/M199 (Sigma). The epithelial origin of cultured cells was confirmed using immunohistochemistry to examine the expression of vimentin and cytokeratins, and only cultures containing >90% epithelial cells were used. ES-2 cells were cultured in DMEM/F12 (Invitrogen). TOV-21G cells were cultured in 1:1 MCDB105/M199 (Sigma). RMG-I cells were cultured in Ham’s F-12 (Invitrogen). OVMANA, OVISE, OVAS, OVTOKO, OVSAYO, KK, and SMOV-2d cells were cultured in RPMI 1640 (Invitrogen). NOSE and cancer cell lines were cultured with 10% heat-inactivated fetal bovine serum and 1% penicillin-streptomycin solution (Invitrogen).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the mirVana miRNA Isolation Kit (ABI). RNA quality were inspected on a 2100 Bioanalyzer (Agilent).
Label biotin
Label protocol According to Illumina protocol.
 
Hybridization protocol According to Illumina protocol.
Scan protocol According to Illumina protocol.
Description Normal ovarian surface epithelium (NOSE) cell culture, biological rep3
Data processing The image data were compiled into a project using Beadstudio software gene expression module version 3.2.7. No normalization was used. The data was exported as txt files using the build-in function of export to GeneSpring GX format. The option of sample probe profile was chosen. Data were subsequently quantile normalized for the analysis.
 
Submission date Jun 12, 2009
Last update date Jan 28, 2010
Contact name Chad Creighton
E-mail(s) creighto@bcm.tmc.edu
Organization name Baylor College of Medicine
Department Biostatistics, Ducan Cancer Center
Street address One Baylor Plaza, Mail Stop: BCM305
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL6947
Series (2)
GSE16570 Gene expression analyses of ovarian clear cell cancer cell lines
GSE16574 Gene expression analyses of putative miRNA targets in ovarian clear cell cancer cell lines

Data table header descriptions
ID_REF
VALUE quantile-normalized signal intensity

Data table
ID_REF VALUE
ILMN_1802380 906.1228
ILMN_1893287 48
ILMN_1736104 46.4
ILMN_1792389 56.9
ILMN_1854015 71.5318
ILMN_1904757 54.125
ILMN_1740305 51.3
ILMN_1665168 47.1
ILMN_2375156 79.8462
ILMN_1705423 55.2
ILMN_1716072 45.8
ILMN_1697642 953.8436
ILMN_1788184 57.66
ILMN_1681845 1664.1435
ILMN_1823296 45.4
ILMN_1889845 44.5
ILMN_1746923 47.4
ILMN_1690979 73.2
ILMN_1811114 48.5
ILMN_1660729 45.05

Total number of rows: 48803

Table truncated, full table size 936 Kbytes.




Supplementary file Size Download File type/resource
GSM416671.txt.gz 677.1 Kb (ftp)(http) TXT
Processed data included within Sample table

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