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Sample GSM213688 Query DataSets for GSM213688
Status Public on May 29, 2008
Title SG_1P{hsGAL4}89_14APF_rep1
Sample type RNA
 
Source name salivary glands expressing GAL4 from one copy of P{GAL4-Hsp70.PB}89-2-1, heat shocked, dissected 14 hours APF
Organism Drosophila melanogaster
Characteristics Salivary glands from animals carrying one copy of P{GAL4-Hsp70.PB}89-2-1, dissected at 14 hours after puparium formation.
Treatment protocol Animals were subjected to a 30-min heat shock treatment at 37 °C at 9 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 (Quiagen, 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 (http://www.affymetrix.com/support/technical/manual/expression_manual.affx).
 
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 animals carrying one copy of P{GAL4-Hsp70.PB}89-2-1, heat shocked at 9 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 145.
 
Submission date Jul 27, 2007
Last update date Aug 28, 2018
Contact name Michael Lehmann
E-mail(s) mlehmann@uark.edu
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 (2)
GSE8620 GAL4-responsive genes in larval salivary glands of late Drosophila prepupae
GSE8623 Senseless-responsive and GAL4-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 211.625
AFFX-BioB-M_at 223.124
AFFX-BioB-3_at 231.809
AFFX-BioC-5_at 605.487
AFFX-BioC-3_at 857.189
AFFX-BioDn-5_at 1607.54
AFFX-BioDn-3_at 2620.78
AFFX-CreX-5_at 7651.64
AFFX-CreX-3_at 7402.27
AFFX-DapX-5_at 516.502
AFFX-DapX-M_at 1089.78
AFFX-DapX-3_at 2041.31
AFFX-LysX-5_at 75.7264
AFFX-LysX-M_at 112.859
AFFX-LysX-3_at 373.749
AFFX-PheX-5_at 126.788
AFFX-PheX-M_at 214.214
AFFX-PheX-3_at 264.899
AFFX-ThrX-5_at 145.349
AFFX-ThrX-M_at 244.758

Total number of rows: 18952

Table truncated, full table size 358 Kbytes.




Supplementary file Size Download File type/resource
GSM213688.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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