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Sample GSM710185 Query DataSets for GSM710185
Status Public on Dec 31, 2012
Title Blood_ACTH_0_probe1_rep1
Sample type RNA
 
Source name blood
Organism Ovis aries
Characteristics breed: Sarda sheep
treatment: injected with ACTH
fed: basal diet
Extracted molecule total RNA
Extraction protocol The extraction of RNA from blood samples was performed with PAXgeneTM blood RNA kit (PreAnalitiX GmbH, Hombrechtikon, Switzerland) following the manufacturer’s instructions.
Label Cy5
Label protocol One-hundred ng of each pool were submitted to double round of amplification using Amino Allyl MessageAmpTM II aRNA Amplification Kit (Ambion, Inc.). At the end of amplification protocol aRNA was labeled with Cy5 dye
 
Hybridization protocol Hybridizations were performed according to the standard protocol supplied with CustomArrayTM 90K (CombiMatrix Irvine, CA, USA). Probes were designed from 12194 UniGenes (NCBI - Build #13) by mean of OligoWiz 2.0 software (Wernersson and Nielsen, 2005). For each Unigene, 2 nonredundant 35-40mer probes were spotted in triplicate on the chip. Bacterial and plant probes were also spotted on the slide as negative control.
Scan protocol The microarray was scanned using a Perkin Elmer laser scanner and data were extracted from the image using CombiMatrix Microarray Imager Software (CombiMatrix Irvine, CA, USA).
Data processing A quantile normalization algorithm was applied as described in Bolstad (2003). This method is a generalization of standard median normalization techniques which match only the 50% quantile of each sample’s signal distribution. Afterwards an in-slide replicates analysis from Midas was used to reduce data redundancy. To evaluate the significant over and under expressed genes between experimental groups, the ratios of T3 to T0 and of T51 to T0 were first calculated for each gene within replicates and data were log(2) transformed to ensure variance homogeneity. Finally, a tab delimited file was imported to MeV software (v 4.6- http://www.tm4.org/mev/; Saeed et al., 2003) and used to perform one-way ANOVA with group as fixed factor. P-values were based on permutation test, with 1000 permutations, and Bonferroni correction was applied setting alpha (critical p-value) at 0.001.
 
Submission date Apr 15, 2011
Last update date Dec 31, 2012
Contact name alberto Pallavicini
E-mail(s) pallavic@units.it
Phone +39 0405588736
Organization name University of Trieste
Department Life Sciences
Lab Genetics
Street address via Giorgierei 5
City Trieste
ZIP/Postal code 34100
Country Italy
 
Platform ID GPL13418
Series (1)
GSE28667 Dietary administration of botanicals to modulate gene expression in peripheral blood cells of sheep under ACTH challenge

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
AB005283_1 791
AB011671_1 1351
AB018478_1 749
AB058897_1 1382
AB070717_1 3116
AB103064_1 3969
AB262769_1 1449
AF001899_1 2145
AF004024_1 285
AF009037_1 3663
AF019622_1 670
AF019758_1 3470
AF024645_1 36700
AF025303_1 295
AF027970_1 1040
AF030005_1 816
AF030006_1 1928
AF030008_1 411
AF030009_1 1567
AF030010_1 388

Total number of rows: 12193

Table truncated, full table size 183 Kbytes.




Supplementary file Size Download File type/resource
GSM710185_ACTH_T0_A_1.TXT.gz 7.7 Mb (ftp)(http) TXT
Processed data included within Sample table

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