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Sample GSM756733 Query DataSets for GSM756733
Status Public on Aug 03, 2012
Title PBMC_145_SFA_baseline
Sample type RNA
 
Source name peripheral blood mononuclear cells (PBMCs), before intervention (baseline)
Organism Homo sapiens
Characteristics gender: male
age: 40-65 yrs
health state: Abdominally overweight
cell type: peripheral blood mononuclear cells
diet: saturated fat
Treatment protocol Subjects consumed a completely controlled saturated fat (SFA)-rich diet, a SFA-by-MUFA-replaced diet (MUFA diet) or a MED diet for 8 weeks. Peripheral mononuclear cells PBMCs were collected before and after intervention.
Growth protocol Abdominally overweight subjects, both males and females aged between 45-60 years, participated in this study. All subjects gave written informed consent to participate in the study and the study protocol was approved by the Medical Ethical Committee of Wageningen University, the Netherlands.
Extracted molecule total RNA
Extraction protocol PBMCs were isolated from fasting whole blood samples by using the BD Vacutainer Cell Preparation Tubes. Total RNA was isolated of all PBMC samples by using the Qiagen RNeasy Micro kit (Qiagen, Venlo, Netherlands). The RNA yield was quantified with a Nanodrop ND 1000 spectrophotometer (Nanodrop Technologies, Wilmington, DE), and RNA integrity was checked on an Agilent 2100 bioanalyzer with RNA 6000 Nano chips (Agilent Technologies, South Queensferry, United Kingdom). Samples were only accepted for microarray analyzes if the RNA integrity number (RIN) was > 8.
Label biotin
Label protocol The Ambion MessageAmp aRNA Amplification Kit was used to prepare labelled cRNA from 500ng of total RNA. The protocol was conducted using the reagents provided by Ambion (P/N 1751), as per the manufacturer's instructions.
 
Hybridization protocol Hybridisation of 10ug cRNA was done overnight for 16 hours at 45ÂșC in a Hybridisation Oven 640 (Affymetrix). The protocol was conducted as described in the Genechip Expression Analysis Technical Manual, section 2 (Eukaryotic Sample and Array Processing), chapter 2 (Eukaryotic Target Hybridization) (P/N 701027, revision 5).
Scan protocol Arrays were scanned on an Affymetrix 3000 7G scanner, as described in the Genechip Expression Analysis Technical Manual, section 2 (Eukaryotic Sample and Array Processing), chapter 2 (Eukaryotic Arrays: Washing, Staining and Scanning (P/N 701028, revision 5).
Data processing Expression estimates were calculated applying the RMA algorithm in the Bioconductor library 'Affy'.
 
Submission date Jul 08, 2011
Last update date Aug 03, 2012
Contact name Guido Hooiveld
E-mail(s) [email protected]
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 GPL7020
Series (1)
GSE30509 Effects of a diet high in monounsaturated fat and a full Mediterranean diet on PBMC whole genome gene expression and plasma proteins

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

Data table
ID_REF VALUE
1007_s_at 5.791406553
1053_at 6.535005589
117_at 6.61743312
121_at 6.51977654
1255_g_at 2.116803882
1294_at 7.780858934
1316_at 3.738133354
1431_at 2.485171625
1487_at 6.20986624
1494_f_at 3.748666838
1552263_at 7.85122099
1552269_at 1.462916015
1552272_a_at 4.145065875
1552278_a_at 2.965720366
1552280_at 2.781060754
1552281_at 4.567975587
1552283_s_at 3.15546094
1552286_at 5.419485517
1552287_s_at 6.704837058
1552291_at 4.865380795

Total number of rows: 23941

Table truncated, full table size 579 Kbytes.




Supplementary file Size Download File type/resource
GSM756733.CEL.gz 1.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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