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Sample GSM213687 Query DataSets for GSM213687
Status Public on May 29, 2008
Title SG_P{hsGAL4}89_14APF_rep1
Sample type RNA
 
Source name salivary glands expressing GAL4 from P{hs-GAL4}89, heat shocked, dissected 14 hours APF
Organism Drosophila melanogaster
Characteristics Salivary glands of animals carrying two copies of P{GAL4-Hsp70.PB}89-2-1, 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 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 two copies 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 241.813
AFFX-BioB-M_at 293.007
AFFX-BioB-3_at 277.091
AFFX-BioC-5_at 738.08
AFFX-BioC-3_at 973.705
AFFX-BioDn-5_at 2158.32
AFFX-BioDn-3_at 2973.22
AFFX-CreX-5_at 7245.1
AFFX-CreX-3_at 7691.77
AFFX-DapX-5_at 419.416
AFFX-DapX-M_at 959.392
AFFX-DapX-3_at 1661.8
AFFX-LysX-5_at 79.6364
AFFX-LysX-M_at 102.561
AFFX-LysX-3_at 419.676
AFFX-PheX-5_at 101.002
AFFX-PheX-M_at 187.29
AFFX-PheX-3_at 281.869
AFFX-ThrX-5_at 123.991
AFFX-ThrX-M_at 244.406

Total number of rows: 18952

Table truncated, full table size 358 Kbytes.




Supplementary file Size Download File type/resource
GSM213687.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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