NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM215856 Query DataSets for GSM215856
Status Public on Mar 20, 2008
Title SG_Fkh_14APF_rep1
Sample type RNA
 
Source name fkh-expressing salivary glands, heat shocked, dissected at 14 hours after puparium formation
Organism Drosophila melanogaster
Characteristics Salivary glands of strain P{hs-Fkh111}, heat shocked, dissected at 14 hours after puparium formation.
Treatment protocol Animals were subjected to a 30-min heat shock treatment at 37 °C at 9.5 hours after puparium formation. Salivary glands were dissected for RNA extraction at 14 hours after puparium formation.
Growth protocol Animals were kept at 25 °C, except during heat shock period.
Extracted molecule total RNA
Extraction protocol Salivary glands were dissected on ice and directly transferred to TRIzol Reagent (Invitrogen, Carlsbad, California). To support lysis of the tissue, the mixture was subjected to vigorous vortexing. Total RNA was isolated according to the instructions of the manufacturer. As a last step of the extraction procedure, the RNA was purified using an RNeasy Minikit (Qiagen, Hilden, Germany).
Label biotin
Label protocol Biotin-labeled cRNA was produced using the One-Cycle Eukaryotic Target Labeling Assay recommended by Affymetrix. Labeling was carried out exactly as specified in the instructions manual, section 2.
 
Hybridization protocol Hybridization was performed following the instructions provided in the Affymetrix Manual (Section 2), using a Fluidics Station 450 and the Midi_euk2 v3 protocol.
Scan protocol GeneChips were scanned using the Affymetrix Genechip 3000 Scanner 7G and Genechip Operation Software (GCOS) v. 1.4.
Description Salivary glands from P{hs-Fkh111} animals heat shocked at 9.5 hours after puparium formation and dissected at 14 hours after puparium formation.
Data processing The data were processed and normalized using dChip 2006. The median intensity of the baseline assay used for normalization was 134.
 
Submission date Aug 08, 2007
Last update date Aug 28, 2018
Contact name Michael Lehmann
E-mail(s) [email protected]
Phone 479-575-3688
Organization name University of Arkansas
Department Biological Sciences
Street address SCEN 601
City Fayetteville
State/province AR
ZIP/Postal code 72701
Country USA
 
Platform ID GPL1322
Series (1)
GSE8722 Fork head-responsive genes in larval salivary glands of late Drosophila prepupae
Relations
Reanalyzed by GSE119084

Data table header descriptions
ID_REF
VALUE dChip-calculated signal intensity

Data table
ID_REF VALUE
AFFX-BioB-5_at 325.535
AFFX-BioB-M_at 424.095
AFFX-BioB-3_at 330.813
AFFX-BioC-5_at 857.595
AFFX-BioC-3_at 1240.34
AFFX-BioDn-5_at 2700.35
AFFX-BioDn-3_at 3576.25
AFFX-CreX-5_at 10140.9
AFFX-CreX-3_at 10435.6
AFFX-DapX-5_at 514.567
AFFX-DapX-M_at 1272.65
AFFX-DapX-3_at 1920.85
AFFX-LysX-5_at 98.8397
AFFX-LysX-M_at 133.284
AFFX-LysX-3_at 448.591
AFFX-PheX-5_at 153.144
AFFX-PheX-M_at 230.077
AFFX-PheX-3_at 394.63
AFFX-ThrX-5_at 123.873
AFFX-ThrX-M_at 316.738

Total number of rows: 18952

Table truncated, full table size 358 Kbytes.




Supplementary file Size Download File type/resource
GSM215856.CEL.gz 3.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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