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Sample GSM561159 Query DataSets for GSM561159
Status Public on Jun 01, 2012
Title Control Fish Replicate2
Sample type RNA
 
Channel 1
Source name whole fish 7 day post-fertilization
Organism Danio rerio
Characteristics condition: Developing fish maintained in egg water (with 0.05% ethanol as vehicle)
Treatment protocol Developing zebrafish were exposed to 500, 1500 and 4500 µg/L BPA for 7 days from 3 hour post-fertilization onwards groups of four zebrafishes. All control fish were maintained in egg water with 0.05% ethanol (vehicle).
Growth protocol Zebrafish were maintained at room temperature (26°C + 1°C)
Extracted molecule total RNA
Extraction protocol Total RNA of tissue samples were extracted using Trizol reagent (Invitrogen) according to the manufacturers instructions.
Label Cy5
Label protocol For fluorescence labeling of cDNAs, 10 µg of total RNA from the reference and experimental samples were reverse transcribed in the presence of Cy3-dUTP and Cy5-dUTP (Amersham Inc.), respectively. Reference RNA was obtained by pooling male and female whole adult total RNA at a ratio of 9:1 respectively. Labeled cDNA were concentrated, and resuspended in DIG EasyHyb (Roche Applied Science) buffer for hybridization.
 
Channel 2
Source name Whole Fish
Organism Danio rerio
Characteristics reference: Reference RNA was obtained by pooling 9:1 ratio of male and female total RNA extracted from whole adult wild-type zebrafish.
Growth protocol Zebrafish were maintained at room temperature (26°C + 1°C)
Extracted molecule total RNA
Extraction protocol Total RNA of tissue samples were extracted using Trizol reagent (Invitrogen) according to the manufacturers instructions.
Label Cy3
Label protocol For fluorescence labeling of cDNAs, 10 µg of total RNA from the reference and experimental samples were reverse transcribed in the presence of Cy3-dUTP and Cy5-dUTP (Amersham Inc.), respectively. Reference RNA was obtained by pooling male and female whole adult total RNA at a ratio of 9:1 respectively. Labeled cDNA were concentrated, and resuspended in DIG EasyHyb (Roche Applied Science) buffer for hybridization.
 
 
Hybridization protocol The respective paired Cy5- labeled cDNAs from control or treated sample and Cy3-labeled cDNAs from reference samples were co-hybridized on a single array at 42°C for 16 h in a hybridization chamber (MAUI, USA) on a glass array spotted with 22,776 zebrafish oligo probes.
Scan protocol The arrays were scanned using the GenePix 4000B microarray scanner (Axon Instruments, USA) and the generated images with their fluorescence signal intensities were analyzed using GenePix Pro 4.0 image analysis software (Axon Instruments, USA).
Description Biological replicate 2 of 5: control fish maintained in egg water (with 0.05% ethanol as vehicle)
Data processing The data were global median normalized. Normalized ratio of means defined by CH1/CH2
 
Submission date Jun 30, 2010
Last update date Jun 01, 2012
Contact name Siew Hong Lam
E-mail(s) [email protected]
Organization name National University of Singapore
Department Biological Sciences
Street address 14 Science Drive 4
City Singapore
ZIP/Postal code 117543
Country Singapore
 
Platform ID GPL10182
Series (1)
GSE22634 Zebrafish toxicogenomics and phenotypic analyses reveal molecular insights into bisphenol-A (BPA) early-life exposure toxicity.

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio of means defined by CH1/CH2

Data table
ID_REF VALUE
5447308 -0.36506456
5447309 -0.57564855
5447310
5447311
5447312 -0.39716867
5447313 0.07394981
5447314
5447315 -0.041601364
5447316 -0.4369953
5447317
5447318
5447319 -0.3151646
5447320
5447321 -0.41296837
5447322 0.40365446
5447323
5447324
5447325
5447326 0.068608314
5447327 0.60017014

Total number of rows: 23232

Table truncated, full table size 289 Kbytes.




Supplementary file Size Download File type/resource
GSM561159.txt.gz 950.3 Kb (ftp)(http) TXT
Processed data included within Sample table

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