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Sample GSM589906 Query DataSets for GSM589906
Status Public on Dec 01, 2011
Title 0.5uM E 100uM Cyclo rep2
Sample type RNA
 
Channel 1
Source name Drosophila melanogaster, Kc 167 cells, 0.5uM ecdy 100uM cyclo, 4hrs
Organism Drosophila melanogaster
Characteristics cell line: Kc167
tissue: embryo-derived
developmental stage: late embryonic
agent: 0.5uM ecdy 100uM cyclo
time point: 4hrs
cell extraction: The sample had an [RNA] of 4.32 ug per uL and an OD ratio of 2.01. Details:3.5 mL Trizol700uL chloroform2.5 mL isopropanol1.5 mL 75% EtOH-brought up in 40uL Sigma 18 meg-ohm water
Extracted molecule total RNA
Extraction protocol Cultures are grown to a minimum density of 5x10^6 cells per mL prior to extraction. Trizol is used at a ratio of 1 mL per 10^7 cells. Extraction procedure is as described by the manufacturer with centrifugation in a Sorvall SS-34 rotor. Final pellets are air dried and then resuspended in Sigma 18 meg-ohm water to obtain a final RNA concentation of no less than 4ug per uL.
Label Cy5
Label protocol CDMC Direct Labeling Protocol. See http://www.flyarrays.com/ under protocols.
 
Channel 2
Source name Drosophila melanogaster, Kc 167 cells, Ethanol Control
Organism Drosophila melanogaster
Characteristics cell line: Kc167
tissue: embryo-derived
developmental stage: late embryonic
agent: Ethanol Control
cell extraction: The sample had an [RNA] of 4.85 ug per uL and an OD ratio of 2.02.Details:3.5 mL Trizol700uL chloroform2.5 mL isopropanol1.5 mL 75% EtOH-brought up in 40uL Sigma 18 meg-ohm water
Extracted molecule total RNA
Extraction protocol Cultures are grown to a minimum density of 5x10^6 cells per mL prior to extraction. Trizol is used at a ratio of 1 mL per 10^7 cells. Extraction procedure is as described by the manufacturer with centrifugation in a Sorvall SS-34 rotor. Final pellets are air dried and then resuspended in Sigma 18 meg-ohm water to obtain a final RNA concentation of no less than 4ug per uL.
Label Cy3
Label protocol CDMC Direct Labeling Protocol. See http://www.flyarrays.com/ under protocols.
 
 
Hybridization protocol See http://www.flyarrays.com/ under protocols. Modifications by Scott:-use 5uL 50mM EDTA-precipitate probe for at least 1 hour-use 20uL DIG EasyHyb per humidifying well-final hyb volume is 80uL
Scan protocol Images of the hybridized microarrays were obtained using a ScanArray 4000 scanner (Perkin-Elmer) and were quantified using QuantArray 3.0 software (Perkin-Elmer)
Data processing Data were normalized using lowest sub-grid normalization (Yang, 2002) and Genetraffic Duo (Stratagene /Agilent) analysis software.
 
Submission date Sep 01, 2010
Last update date Dec 01, 2011
Contact name Zak Razak
E-mail(s) z.razak@utoronto.ca
Phone 905-569-4664
Fax 905-828-3792
URL http://www.flyarrays.com
Organization name Canadian Drosophila Microarray Centre
Street address 3359 Mississauga Rd
City Mississauga
State/province Ontario
ZIP/Postal code L5L 1C6
Country Canada
 
Platform ID GPL1467
Series (1)
GSE23928 Genome-wide examination of the transcriptional response to ecdysteroids 20-hydroxyecdysone and ponasterone A in Drosophila melanogaster

Data table header descriptions
ID_REF
VALUE LOG 2 ratio (channel 1/ channel 2 , Lowess-normalized)

Data table
ID_REF VALUE
1 0.443155665
2 -0.128513476
3 0.294778175
4 0.187051547
5 -0.11973517
6 0.415289014
7 -0.037555565
8 -0.17786385
9 0.320668546
10 0.588947756
11 -0.115338164
12 0.682072354
13 -0.061896135
14 -0.239629651
15 -0.744863034
16 -0.517314844
17 -0.098011114
18 0.010062325
19 -0.150788961
20 -0.213965959

Total number of rows: 27648

Table truncated, full table size 491 Kbytes.




Supplementary file Size Download File type/resource
GSM589906.txt.gz 3.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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