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Sample GSM2356563 Query DataSets for GSM2356563
Status Public on Feb 12, 2017
Title Subject A_subcutaneous_0 nM dexamethasone
Sample type RNA
 
Source name subcutaneous_0 nM dexamethasone
Organism Homo sapiens
Characteristics subject status: 48yrs, F, AA with BMI 54 (kg/m2)
treatment: dexamethasone
depot: subcutaneous
concentration: 0 nM
tissue: adipose tissue explant
Treatment protocol Media (with same additions/treatments) was exchanged every other day and on the day prior to processing on d7.
Growth protocol organ culture protocol: 300-400 mg of minced adipose tissue fragments (5-10 mg) were placed in organ culture in 15 ml of Medium 199 with the treatments as previously described (Lee et al, Am J Physiol Endocrinol Metab. 2011 Mar;300(3):E571-80)
Extracted molecule total RNA
Extraction protocol Total RNA was isolated with Trizol reagent (Life Technologies, Carlsbad, CA), cleaned with RNeasy MiniElute Cleanup Kit (Qiagen, Germantown, MD).
Label biotin
Label protocol Biotin labeling was performed using the Ambion WT Expression Kit (Life Technologies, Grand Island, NY) according to the manufacturer's protocol, followed by the GeneChip WT Terminal Labeling and Controls Kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol The labeled, fragmented DNA was hybridized to the GeneChip Human Gene 1.0 ST Array for 18 hours in a GeneChip Hybridization oven 640 at 45oC with rotation (60 rpm). The hybridized samples were washed and stained using an Affymetrix fluidics station 450.
Scan protocol After staining, microarrays were immediately scanned using an Affymetrix GeneArray Scanner 3000 7G Plus.
Description A-S1
Gene expression data from subcutaneous adipose tissue explant treated with 0 nM dexamethasone.
Data processing Raw Affymetrix CEL files were normalized to produce gene-level expression values using the implementation of the Robust Multiarray Average (RMA) in the affy Bioconductor package (version 1.36.1) and an Entrez Gene-specific probeset mapping (version 14.0.0) from the Molecular and Behavioral Neuroscience Institute (Brainarray) at the University of Michigan. NOTE: RMA normalization was performed using additional samples, and so the gene expression values in this GEO record cannot be reproduced exactly from these samples alone.
 
Submission date Oct 20, 2016
Last update date Jun 25, 2019
Contact name Boston University Microarray and Sequencing Resource
E-mail(s) [email protected]
Organization name Boston University
Department Microarray and Sequencing Resource
Street address 72 East Concord Street, E631
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL15034
Series (1)
GSE88966 Depot dependent effects of dexamethasone on gene expression in human omental and abdominal subcutaneous adipose tissues from obese women.

Data table header descriptions
ID_REF
VALUE log2-transformed, RMA-normalized Entrez Gene expression values

Data table
ID_REF VALUE
100009676_at 6.716436122
10000_at 8.709944475
10001_at 8.104834177
10002_at 4.223537997
100033413_at 5.984128944
100033414_at 5.007594003
100033416_at 5.626864962
100033418_at 6.766103262
100033420_at 8.049247678
100033422_at 2.558992447
100033423_at 3.675812352
100033424_at 2.739318601
100033425_at 2.639461438
100033426_at 9.953687579
100033427_at 11.19253016
100033428_at 2.354362812
100033430_at 2.184663473
100033431_at 7.924120821
100033432_at 4.938330801
100033433_at 3.351776886

Total number of rows: 19741

Table truncated, full table size 401 Kbytes.




Supplementary file Size Download File type/resource
GSM2356563_SF_A6_A-S1.CEL.gz 3.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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