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Sample GSM758790 Query DataSets for GSM758790
Status Public on Oct 01, 2011
Title 12 hpf control [miRNA]
Sample type RNA
 
Source name whole embryo 12 hpf
Organism Danio rerio
Characteristics strain: Tropical 5D
agent: control
dose: n/a
locomotion phenotype: Normal
collection time: 12 hpf
Treatment protocol Groups of embryos were waterborne exposed to 300 mM ethanol (absolute ethyl alcohol USP, 200 proof) in buffered embryo medium or embryo medium alone in 20-ml glass vials sealed with Teflon-lined lids to prevent volatilization. Each exposure group was considered a single replicate. Based on previous studies, embryos were exposed to ethanol from 4-24 hpf, rinsed and embryo homogenate was collected at 12, 24, 36, or 48 hpf.
Growth protocol Adult Tropical 5D strain zebrafish (Danio rerio) were raised according to Institutional Animal Care and Use Committee protocols in the Sinnhuber Aquatic Research Laboratory at Oregon State University. Adults were maintained on a 14 h light/10 h dark schedule on a recirculating system in which water was maintained at 28±1 °C with a pH of 7.0±0.2. Following adult spawns, embryos were collected, rinsed, and housed at 28±1 °C in pools of 75 embryos until the start of the experiment.
Extracted molecule total RNA
Extraction protocol miRNA was isolated using a miRNeasy kit (Qiagen) from pooled tissue (75 embryos) harvested at 12-48 hpf (n=2).
Label Cy3
Label protocol cDNA synthesis, labeling and hybridization were performed by LC Sciences as per the manufacturer’s specifications.
 
Hybridization protocol cDNA synthesis, labeling and hybridization were performed by LC Sciences as per the manufacturer’s specifications. Labeled cDNA samples were hybridized to miRZebrafish arrays (probe content reflects miRBase release 12.0) and images were collected using a laser scanner (GenePix 4000B, Molecular Device) and digitized using Array-Pro image analysis software (Media Cybernetics).
Scan protocol cDNA synthesis, labeling and hybridization were performed by LC Sciences as per the manufacturer’s specifications. Labeled cDNA samples were hybridized to miRZebrafish arrays (probe content reflects miRBase release 12.0) and images were collected using a laser scanner (GenePix 4000B, Molecular Device) and digitized using Array-Pro image analysis software (Media Cybernetics).
Description This sample is comprised of 75 pooled embryos exposed to embryo medium control from 4-12 hpf and harvested at 12 hpf. It is a pooled sample comprised of two biological replicates, each from separate pools of 75 embryos.
Raw data file: 07_Z12.0_090073-0126.txt
Data processing Data were background-subtracted, normalized by LOWESS (Locally-weighted Regression), and analyzed for differential expression by t-test (p<0.05). Data processing was performed by LC Sciences using proprietary software (Bolstad, BM et al. 2003. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinfo. 19, 185-193).
 
Submission date Jul 12, 2011
Last update date Oct 01, 2011
Contact name Robert L Tanguay
E-mail(s) robert.tanguay@oregonstate.edu
Phone 541-737-6514
Organization name Oregon State University
Department EMT
Street address 1007 ALS
City Corvallis
State/province OR
ZIP/Postal code 97331
Country USA
 
Platform ID GPL13832
Series (1)
GSE30497 mRNA and miRNA expression analysis of developmental ethanol exposure in zebrafish

Data table header descriptions
ID_REF
VALUE normalized signal

Data table
ID_REF VALUE
2079 33.8888895
1118 34.8511937
3040 37.2037035
167 37.8048977
2099 38.7129626
2089 41.7037036
1138 12.0648146
177 18.3511937
1128 33.4351856
3050 36.3333335
3060 38.933966
157 63.1851855
198 28.5185186
2110 28.8333335
3081 43.9907405
1149 1.703045697
3071 9.304897697
1169 12.8703706
2130 18.4537036
3091 21.6660087

Total number of rows: 2920

Table truncated, full table size 44 Kbytes.




Supplementary file Size Download File type/resource
GSM758790.txt.gz 58.0 Kb (ftp)(http) TXT
Processed data included within Sample table

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