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Sample GSM318869 Query DataSets for GSM318869
Status Public on Oct 30, 2008
Title PHA unstimulated, Tempus, replicate R (Blood_PHA0_ABI_R)
Sample type RNA
 
Source name Peripheral blood
Organism Homo sapiens
Characteristics n/a
Treatment protocol Whole blood from 7 healthy individuals was collected using Li Heparin tubes, and was incubated for 3 hours at room temperature with or without addition of 25 ug/mL of PHA. After incubation, samples were subsequently transferred to either Tempus or PAXgene tubes.
Extracted molecule total RNA
Extraction protocol RNA was extracted at the ITN Central Nucleic Acid Isolation Core facility, Pittsburgh, PA according to the ITN modified method for Tempus. Whole blood samples collected into Tempus vacuette were extracted using ABI Prism 6100 Nucleic Acid PrepStation and using Tempus extraction reagents. The PAXgene whole blood sample were processed using the PAXgene Blood RNA Kit based on the Qiagen method for column purification of nucleic acid.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol. cRNA target amplificationwas performed using the Affymetrix In-vitro Transcription (IVT) Kit followed by a Globin Reduction step.
 
Hybridization protocol Hybridization on Affymetrix HG-U133 2.0 plus array according to manufacturer's instructions.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description PHA unstimulated, Tempus RNA extraction method, replicate R
Data processing The data normalizaion was performed using Bioconductor package THREESTEP(background.method="MASIM", noemalize.method="scaling", summary.method="tukey.biweight").
 
Submission date Sep 09, 2008
Last update date Aug 28, 2018
Contact name Zhong Gao
Organization name Johns Hopkins University
Street address Ross 844 720 Rutland Avenue
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL570
Series (2)
GSE12709 Differential gene expression profiles are dependent upon method of peripheral blood RNA isolation (PHA)
GSE12711 Differential gene expression profiles are dependent upon method of peripheral blood RNA isolation
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE Normalized intensity value

Data table
ID_REF VALUE
1007_s_at 5.10271070248958
1053_at 5.07772737737251
117_at 7.18799283296356
121_at 6.13879787198873
1255_g_at 2.35455511139681
1294_at 5.39792563834037
1316_at 4.36323383367488
1320_at 1.39464592049923
1405_i_at 10.5315164997687
1431_at 2.36821659557876
1438_at 1.40630343112319
1487_at 5.10228852725951
1494_f_at 4.1748295492019
1552256_a_at 3.61216703467521
1552257_a_at 4.5862384649782
1552258_at 3.56389875345312
1552261_at 1.64079654343078
1552263_at 6.83112486630682
1552264_a_at 7.67137116464462
1552266_at 2.38174227299999

Total number of rows: 54675

Table truncated, full table size 1490 Kbytes.




Supplementary file Size Download File type/resource
GSM318869.CEL.gz 7.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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