NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM701169 Query DataSets for GSM701169
Status Public on Oct 15, 2011
Title Renal medulla of hypertensive, m34
Sample type RNA
 
Source name Renal medulla of hypertensive male
Organism Homo sapiens
Characteristics gender: male
tissue: renal medulla
blood pressure: hypertensive
Treatment protocol Tissue was transferred into containers with RNAlater (Ambion) and preserved at 70°C before mRNA extraction.
Growth protocol Approximately 1 cm3 of tissue from the healthy (unaffected by cancer) pole of the kidney was obtained immediately after surgery.
Extracted molecule total RNA
Extraction protocol The RNeasy kit (Qiagen) was used for extraction of total RNA according to the manufacturer's instructions. Medulla and cortex were separated and individual RNA was obtained for each of them.
Label biotin
Label protocol 100ng of total RNA was prepared for hybridization according to the standard Affymetrix protocol (GeneChip Whole Transcript (WT) Sense Target Labeling Assay Manual, version 4, Affymetrix).
 
Hybridization protocol After fragmentation, ssDNA was hybridized to GeneChip Human Gene 1.0 ST Arrays for 17 hr at 45°C. Chips were washed and stained in the Affymetrix GeneChip Fluidics Stations 450. For all of these steps, the GeneChip Hybridization, Wash, and Stain Kit (Affymetrix) was used according to manufacturer’s recommendations (GeneChip Whole Transcript (WT) Sense Target Labelling Assay Manual, version 4, Affymetrix).
Scan protocol The chips were scanned using the GeneChip Scanner 3000 7G 4C (Affymetrix) according to the manufacturer’s recommendations (GeneChip Whole Transcript (WT) Sense Target Labelling Assay Manual, version 4, Affymetrix).
Description Gene expression from male hypertensive patient.
Data processing The samples were individually normalized using robust-multi-array analysis (RMA) in the R application (version 2.11.1). Differentially expressed genes were identified using the moderated two-sample t-test in the Limma package.
 
Submission date Apr 04, 2011
Last update date Oct 15, 2011
Contact name Prof.Brian J Morris
E-mail(s) [email protected]
Organization name University of Sydney
Department Physiology
Lab Basic & Clinical Genomics Lab
Street address Anderson Stuart Building, room N452, University of Sydney
City Sydney
State/province NSW
ZIP/Postal code 2006
Country Australia
 
Platform ID GPL6244
Series (2)
GSE28260 Renal cortex and medulla microRNA and mRNA expression differences between hypertensive and normotensive patients
GSE28360 Renal medulla expression differences between hypertensive and normotensive patients

Data table header descriptions
ID_REF
VALUE RMA-normalized log2 expression value

Data table
ID_REF VALUE
7892501 2.733660462
7892502 4.264564156
7892503 2.572452206
7892504 6.777587607
7892505 1.663583557
7892506 2.919584487
7892507 4.621396746
7892508 5.596145696
7892509 9.643740029
7892510 4.478549827
7892511 2.342413373
7892512 5.355158299
7892513 2.277523642
7892514 7.65823443
7892515 7.204826102
7892516 3.331916188
7892517 6.364531917
7892518 2.321768782
7892519 2.890555705
7892520 8.269318198

Total number of rows: 32321

Table truncated, full table size 627 Kbytes.




Supplementary file Size Download File type/resource
GSM701169.CEL.gz 3.7 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap