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Sample GSM756715 Query DataSets for GSM756715
Status Public on Aug 03, 2012
Title PBMC_113_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 5.915559278
1053_at 6.561269735
117_at 6.598323732
121_at 6.821626151
1255_g_at 2.031483439
1294_at 7.588792813
1316_at 3.920597318
1431_at 2.495532414
1487_at 6.246016158
1494_f_at 3.749011317
1552263_at 8.255704069
1552269_at 1.695440031
1552272_a_at 4.097203517
1552278_a_at 2.882023196
1552280_at 2.859499573
1552281_at 4.841040095
1552283_s_at 3.133243295
1552286_at 5.586782186
1552287_s_at 6.441841806
1552291_at 5.783302658

Total number of rows: 23941

Table truncated, full table size 579 Kbytes.




Supplementary file Size Download File type/resource
GSM756715.CEL.gz 1.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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