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Sample GSM1374068 Query DataSets for GSM1374068
Status Public on Jan 24, 2020
Title PET31_A
Sample type RNA
 
Source name cells from peritoneal dialysis effluent, previous peritonitis, with AlaGln
Organism Homo sapiens
Characteristics cell type: cells isolated from peritoneal effluent of peritoneal dialysis patient
treatment: treatment A - with AlaGln
previous_peritonitis: yes
patient: 18
Treatment protocol No in-vitro treatment was performed. The differential treatment of the isolated cells resulted from treatment with different peritoneal dialysis solutions in the course of the clinical study.
Growth protocol No cell culturing was performed. The used cell material was freshly isolated from peritoneal dialysis effluents.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from peritoneal cells (4 h PET) using RNeasy columns (Qiagen), using 350 µl of RLT buffer (Qiagen) and following the manufacturer's instructions without modifications.
Label biotin
Label protocol 100ng of total RNA were amplified and labeled using the Ambion Whole Transcript Expression Kit (Catalog Number 4425209, Ambion, Austin, TX) and Affymetix GeneChip Whole Transcript Terminal Labeling Kit (Catalog Number 900671, Affymetrix, Santa Clara, CA).
 
Hybridization protocol Affymetrix GeneChip® Human Gene 1.0 ST arrays were washed, stained and scanned according to the protocol described in GeneChip® WT Terminal Labeling and Hybridization User Manual (Fluidics Protocol FS450_0007).
Scan protocol Scanning was done on an Affymetrix GeneChip Scanner 3000 7G, software AGCC 3.1.1.
Description Gene expression data from cells isolated from peritoneal effluent following a single 4 h peritoneal dialysis dwell with added AlaGln in a patient who had previously suffered from peritonitis.
Data processing Samples were normalized via the Comprehensive R based Microarray Analysis web frontend CARMAweb (https://carmaweb.genome.tugraz.at/carma) using the Robust Multiarray Analysis (RMA) algorithm. The algorithm consists of: background correction (subtract the minimal signal intensity), normalization (quantile-quantile normalization) and summarizing the probe set values.
 
Submission date Apr 24, 2014
Last update date Jan 24, 2020
Contact name Klaus Kratochwill
Organization name Medical University of Vienna
Street address Lazarettgasse 14
City Wien
ZIP/Postal code 1090
Country Austria
 
Platform ID GPL11209
Series (1)
GSE57070 Alanyl-glutamine in peritoneal dialysis fluids - a randomized controlled phase I/II trial

Data table header descriptions
ID_REF
VALUE RMA signal intensity on base of log2

Data table
ID_REF VALUE
ENSG00000000003 7.51558899368295
ENSG00000000005 4.38357263909246
ENSG00000000419 9.99988540746816
ENSG00000000457 7.98193784985668
ENSG00000000460 5.57286014291941
ENSG00000000938 10.9470246483393
ENSG00000000971 10.6017239849964
ENSG00000001036 9.42992800260873
ENSG00000001084 7.70581953076987
ENSG00000001167 9.0928620484461
ENSG00000001460 8.24474175478632
ENSG00000001461 8.6310751283068
ENSG00000001497 7.70851172110703
ENSG00000001561 6.90120867924751
ENSG00000001617 7.40748288115044
ENSG00000001626 5.19933155913294
ENSG00000001629 9.97276030877657
ENSG00000001630 4.76889532085146
ENSG00000001631 8.57787035929622
ENSG00000002016 7.69459653888317

Total number of rows: 22197

Table truncated, full table size 712 Kbytes.




Supplementary file Size Download File type/resource
GSM1374068_MJ_03302012_KRA_4_HuGene-1_0-st-v1_.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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