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Sample GSM397756 Query DataSets for GSM397756
Status Public on Jan 04, 2010
Title Drosophila OSS cells_1
Sample type RNA
 
Source name OSS cells
Organism Drosophila melanogaster
Characteristics cell line: OSS
cell type: follicular stem cell
Biomaterial provider Yuzo Niki supplied original starting culture, while cultures utilized in these experiments were grown by Nelson Lau.
Treatment protocol Cells grown in exponential phase in standard medium, no additional treatment
Growth protocol Cells were cultured in 6 well plates, split every 3 days 1:3, and were cultured in Shield and Sang's M3 media supplemented with 10% fetal bovine serum, 1ug/ml insulin, 60ug/ml glutathione, and 5% fly extract.
Extracted molecule total RNA
Extraction protocol Near-confluent wells washed once with 1XPBS, then subject to Trizol extraction to obtain total RNA.
Label Biotin
Label protocol 10 ug of total RNA from each sample was converted to cDNA and then to biotinylated cRNA with the One-Cycle Target Labeling protocol as detailed in the Affymetrix manual for GeneChip® Eukaryotic Labeling Assays for Expression Analysis.
 
Hybridization protocol Hybridization on the Affymetrix Fluidics 450 system was performed with the standard protocol #FS450_0002 as detailed in the program software.
Scan protocol Scanning was performed on the GeneChip ® Scanner 3000 using the preset pixel value and resolution parameters defined in the scanner.
Description OSS cells are a stable cell line derived from follicular stem cells of the Drosophila ovary. The cells express the Fas III gene as a marker of follicle cells, and are described in Niki et. al., Proc Natl Acad Sci USA 2006 Oct 31;103(44): 16325-30.
CEL and DAT files were outputed from scanning and utilized in custom analysis scripts
Data processing Array files were processed with Bioconductor scripts in the R statistical and graphing package.
 
Submission date Apr 25, 2009
Last update date Aug 28, 2018
Contact name Nicolas Robine
Organization name Sloan-Kettering Institute
Department Developmental Biology
Lab Dr. Eric Lai's Lab
Street address 430, East 67th Street, RRL 517
City New York
State/province NY
ZIP/Postal code 10065
Country USA
 
Platform ID GPL1322
Series (1)
GSE15825 An mRNA/3' UTR-directed primary piRNA pathway in Drosophila ovarian somatic cells
Relations
Reanalyzed by GSE119084

Data table header descriptions
ID_REF
VALUE GC-RMA normalized log2 signal

Data table
ID_REF VALUE
1616608_a_at 2.821129204
1622892_s_at 4.134986289
1622893_at 2.437007742
1622894_at 2.399110463
1622895_at 4.087586511
1622896_at 4.273392103
1622897_at 2.388889322
1622898_a_at 4.720144005
1622899_at 2.462920077
1622900_at 2.388889322
1622901_at 2.389177039
1622902_at 2.467608618
1622903_s_at 2.888540557
1622904_at 2.453339889
1622905_at 2.388889322
1622906_at 2.388889322
1622907_at 4.682998038
1622908_a_at 2.449784582
1622909_at 5.41531519
1622910_at 2.391947552

Total number of rows: 18952

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM397756.CEL.gz 1.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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