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Sample GSM619227 Query DataSets for GSM619227
Status Public on Aug 21, 2011
Title Epidydimal white adipose tissue from Casp1-/- after 16 weeks of high fat diet feeding, replicate 2
Sample type RNA
 
Source name Adipose tissue from male Casp1-/- animal (C57/Bl6 background)
Organism Mus musculus
Characteristics strain: C57/Bl6
genotype/variation: Caspase 1 null
gender: male
tissue: epididymal white adipose tissue
Treatment protocol White adipose tissue was dissected from all 3 genotypes after 16 weeks of high fat diet-feeding. Adipose tissue RNA samples from 3-4 mice per experimental group were used for microarray analysis.
Growth protocol Male wild-type (control) (C57/BL6 background) and ASC-/- and Casp1-/- mice (C57/BL6 background), aged 8-12 weeks at the start of the intervention, were maintained on a high fat diet (45 energy% of fat) for 16 weeks. After the diet intervention, mice were killed and the adipose tissue was removed.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared from mouse adipose tissue using TRIzol reagent and whereafter purified total RNA was isolated using Qiagen RNEasy columns. RNA integrity was checked on chip analysis (Agilent 2100 bioanalyzer, Agilent Technologies, Amsterdam, the Netherlands) according to the manufacturer's instructions. RNA was judged as suitable for array hybridization only if samples exhibited intact bands corresponding to the 18S and 28S ribosomal RNA subunits, and displayed no chromosomal peaks or RNA degradation products (RNA Integrity Number > 8.0).
Label biotin
Label protocol All target labeling reagents were purchased from Affymetrix (Santa Clara, CA). Double-stranded cDNAs were synthesized from 1ug total RNA through reverse transcription with an oligo-dT primer containing the T7 RNA polymerase promoter and double strand conversion using the cDNA Synthesis System. Biotin-labeled cRNA was generated from the cDNA and used to probe Affymetrix Mouse Genome HT_MG-430 PM arrays.
 
Hybridization protocol The GeneChip HT MG-430 PM 24 Array Plate consists of 24 single MG-430 PM arrays arranged into standard 96 well plate format. Array hybridization, washing and scanning were performed according to the manufacturer’s recommendations on a GeneTitan Instrument.
Scan protocol Arrays were scanned on an Affymetrix GeneTitan instrument.
Data processing Expression estimates were calculated using RMA in Bioconductor.
 
Submission date Nov 08, 2010
Last update date Aug 21, 2011
Contact name Guido Hooiveld
E-mail(s) guido.hooiveld@wur.nl
Organization name Wageningen University
Department Div. Human Nutrition & Health
Lab Nutrition, Metabolism & Genomics Group
Street address HELIX, Stippeneng 4
City Wageningen
ZIP/Postal code NL-6708WE
Country Netherlands
 
Platform ID GPL11180
Series (1)
GSE25205 The inflammasome is a central player in the induction of obesity and insulin resistance

Data table header descriptions
ID_REF
VALUE RMA signal (as log2)

Data table
ID_REF VALUE
1415670_PM_at 9.731011267
1415671_PM_at 11.02165349
1415672_PM_at 10.09451698
1415673_PM_at 8.838491631
1415674_PM_a_at 9.516882078
1415675_PM_at 8.301780905
1415676_PM_a_at 10.21862457
1415677_PM_at 8.603809434
1415678_PM_at 10.67269345
1415679_PM_at 10.96316223
1415680_PM_at 8.979517534
1415681_PM_at 9.19067392
1415682_PM_at 7.154832523
1415683_PM_at 10.73197261
1415684_PM_at 8.286314069
1415685_PM_at 7.858640958
1415686_PM_at 9.257484879
1415687_PM_a_at 11.93287618
1415688_PM_at 10.06009256
1415689_PM_s_at 8.205453748

Total number of rows: 45141

Table truncated, full table size 1159 Kbytes.




Supplementary file Size Download File type/resource
GSM619227.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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