NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM230684 Query DataSets for GSM230684
Status Public on Jan 02, 2008
Title Reselected MA low line C2 (2482.VC2-1)
Sample type RNA
 
Source name Wing discs MA C2 line
Organism Drosophila melanogaster
Characteristics Reselected Massachussetts low angular offset
Age: 3rd instar larvae median age 6.2 hr prior to pupariation.
Treatment protocol Larvae were dissected in 30 μl drops of cold PBS on siliconized slides, with needle-tip tweezers where wing disks were rapidly excised and cleaned with tungsten wire needles. Each pair of disks was then transferred from the needle tip to the bottom of a 0.5 ml microcentrifuge tube in dry ice, where 100 disks were collected in single microcentrifuge tubes.
Growth protocol Lines H and L were derived from a wild Massachusetts population sample by 20 generations of divergent selection, then isogenized. H and L were then crossed to make hybrid populations A-D. After 34 generations of genomic mingling, hybrid lines were divergently selected for 25 generations, then inbred for 10. The California lines were selected from a separate population. Flies were cultured at 20ºC on cornmeal agar medium.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description Gene expression data from wing discs.
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 2500.
 
Submission date Sep 20, 2007
Last update date Aug 28, 2018
Contact name Ralph J Greenspan
E-mail(s) greenspan@nsi.edu
Phone 858-626-2075
Organization name The Neurosciences Institute
Street address 10640 John Jay Hopkins Dr.
City San Diego
State/province CA
ZIP/Postal code 92121
Country USA
 
Platform ID GPL1322
Series (1)
GSE9107 Expression data of Drosophila 3rd instar larval wing discs taken from strains selected for wing shape.
Relations
Reanalyzed by GSE119084

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)

Data table
ID_REF VALUE ABS_CALL
AFFX-BioB-5_at 1627.6 P
AFFX-BioB-M_at 1625.4 P
AFFX-BioB-3_at 1267.9 P
AFFX-BioC-5_at 3840.7 P
AFFX-BioC-3_at 3548.9 P
AFFX-BioDn-5_at 7449.7 P
AFFX-BioDn-3_at 25988.3 P
AFFX-CreX-5_at 51080.7 P
AFFX-CreX-3_at 70764 P
AFFX-DapX-5_at 34.1 A
AFFX-DapX-M_at 117.6 A
AFFX-DapX-3_at 32.9 A
AFFX-LysX-5_at 3.3 A
AFFX-LysX-M_at 216.8 A
AFFX-LysX-3_at 170.5 A
AFFX-PheX-5_at 25.2 A
AFFX-PheX-M_at 18.3 A
AFFX-PheX-3_at 173.3 A
AFFX-ThrX-5_at 30.8 A
AFFX-ThrX-M_at 134.6 A

Total number of rows: 18952

Table truncated, full table size 359 Kbytes.




Supplementary file Size Download File type/resource
GSM230684.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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