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Sample GSM419073 Query DataSets for GSM419073
Status Public on Nov 17, 2009
Title Hippocampus right animal 3
Sample type other
 
Channel 1
Source name Hippocampus right hand side
Organism Rattus norvegicus
Characteristics strain: Sprague-Dawley
gender: male
developmental stage: Adult
tissue: hippocampus
hemisphere: Right
molecule: microRNA
Growth protocol Animals were kept under normal day/night and dairy conditions with unlimited access to food and water.
Extracted molecule other
Extraction protocol RNeasy Lipid Tissue Mini Kit (Qiagen) following manufacturer's instructions
Label Alexa Fluor® 5 fluorophor
Label protocol 600 ng microRNA sample were poly-A tailed and tagged with the sequence tag for the Alexa Fluor® 5 fluorophor using the NCode™ miRNA Labeling System (Invitrogen). Universal reference were labeled with Alexa Fluor® 3.
 
Channel 2
Source name universal brain reference
Organism Rattus norvegicus
Characteristics sample type: Invitrogen universal brain reference small RNA (>200 nt in length)
Extracted molecule other
Extraction protocol RNeasy Lipid Tissue Mini Kit (Qiagen) following manufacturer's instructions
Label Alexa Fluor® 5 fluorophor
Label protocol 600 ng microRNA sample were poly-A tailed and tagged with the sequence tag for the Alexa Fluor® 5 fluorophor using the NCode™ miRNA Labeling System (Invitrogen). Universal reference were labeled with Alexa Fluor® 3.
 
 
Hybridization protocol Samples were hybridized against the reference overnight to NCode™ Multi-Species miRNA Microarrays (Invitrogen, Carlsbad, CA, USA) using the NCode™ Multi-Species miRNA Microarrays Kit (Invitrogen, Carlsbad, CA, USA) following the instructions given by the manufacturer. Arrays were then hybridized on a MAUI hybridization station (BioMicro Systems, Inc, Salt Lake City, UT, USA) with Alexa Fluor® 3 and Alexa Fluor® 5 capture reagents and washed.
Scan protocol Scanned using an Agilent DNA microarray scanner.
Images were processed using GenePix Pro software (Molecular Devices, Sunnyvale, CA, USA).
Description Biological replicate 2 of 4.
Data processing Background adjusted using “normexp” with an offset of 50. Print-tip-loess normalization was used to adjust data within each array and subsequent Gquantile normalization to allow comparisons between arrays. Thelimma package from BioConductor was used in R.
 
Submission date Jun 19, 2009
Last update date Nov 17, 2009
Contact name Thomas Werge
Phone +45 4633 4968
Organization name Psychiatric Center, Sct. Hans Hospital
Department Institute of biological Psychiatry
Street address Boserupvej 2
City Roskilde
ZIP/Postal code Dk-4000
Country Denmark
 
Platform ID GPL8745
Series (1)
GSE16725 Regional brain expression maps for microRNAs in rats

Data table header descriptions
ID_REF
VALUE gquantile normalized log 2 ratio (test sample/universal reference)

Data table
ID_REF VALUE
1030 -1.45291782
1231 0.304222402
1431 -0.39131065
1268 -0.122296795
1085 -0.174071037
1421 -1.283473812
1033 -0.901558683
1064 -2.319685485
1297 0.76655093
1164 -0.084546775
1163 -0.010615231
1072 -0.708480651
1213 -0.033914665
1377 1.299036804
1384 -0.355384999
1106 0.20120046
1253 -0.090568311
1225 1.579618633
1272 -0.076867672
1031 -1.255927735

Total number of rows: 236

Table truncated, full table size 4 Kbytes.




Supplementary file Size Download File type/resource
GSM419073.gpr.gz 377.3 Kb (ftp)(http) GPR
Processed data included within Sample table

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