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Sample GSM756721 Query DataSets for GSM756721
Status Public on Aug 03, 2012
Title PBMC_120_SFA_baseline
Sample type RNA
 
Source name peripheral blood mononuclear cells (PBMCs), before intervention (baseline)
Organism Homo sapiens
Characteristics gender: female
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 5.995743603
1053_at 6.324916716
117_at 7.091722776
121_at 6.502245505
1255_g_at 1.987029196
1294_at 7.962026949
1316_at 3.738991863
1431_at 2.355068966
1487_at 6.291088255
1494_f_at 3.560492556
1552263_at 7.86067457
1552269_at 1.729243147
1552272_a_at 4.240428525
1552278_a_at 2.975679371
1552280_at 2.659833667
1552281_at 4.231418653
1552283_s_at 2.964111694
1552286_at 5.35868142
1552287_s_at 6.76145948
1552291_at 4.925343745

Total number of rows: 23941

Table truncated, full table size 579 Kbytes.




Supplementary file Size Download File type/resource
GSM756721.CEL.gz 1.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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