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Sample GSM215000 Query DataSets for GSM215000
Status Public on Nov 19, 2007
Title Neutrophils before exercise 10
Sample type RNA
 
Source name Human netrophils before exercise
Organism Homo sapiens
Characteristics neutrophil, healthy male, age 19
before-exercise
Extracted molecule total RNA
Extraction protocol Neutrophils were isolated using OptiPrepÒ Density Gradient Medium (SIGMA). Using hematoxylin staining, we determined that this approach to neutrophil isolation consistently yielded ≥ 98% purification. Total RNA was extracted using TRIzol® reagent and purified using the RNeasy Midi columns method (Qiagen, Valencia, CA)
Label biotin
Label protocol 2 μg total RNA was used as a template for double‑stranded cDNA synthesis. Single-stranded then double-stranded cDNA was synthesized from the poly A spike-in controls, and mRNA present in the isolated total RNA using the SuperScript Double-Stranded cDNA Synthesis Kit (Invitrogen Corp., Carlsbad, CA), and a T-7-oligo(dT) primer (Integrated DNA Technologies Inc.,Coralville,IA) that contains a T7 RNA polymerase promoter site added to it’s 3' end. A portion of the resulting double-stranded cDNA was used as a template to generate biotin-tagged cRNA from an in vitro transcription reaction (IVT), using the Affymetrix GeneChip® IVT Labeling Kit.
 
Hybridization protocol 10 µg of fragmented target cRNA was hybridized at 45°C with rotation for 16 hours (Affymetrix GeneChip® Hybridization Oven 640) to probe sets present on an Affymetrix U133+2 arrays.
Scan protocol The GeneChip® arrays were washed and then stained (SAPE, streptavidin-phycoerythrin) on an Affymetrix Fluidics Station 450, followed by scanning on a GeneChip® Scanner 3000.
Description no additional
Data processing The results were quantified and analyzed using GCOS 1.4 software (Affymetrix, Inc.) using default values (Scaling Target Signal Intensity=500; Normalization, All probe sets; Parameters, all set at default values). The microarray data was analyzed using ArrayAssistÒ version 4.0.3 (STRATAGENEÒ ). We normalized the data using GC-RMA.
 
Submission date Aug 02, 2007
Last update date Aug 28, 2018
Contact name Shlomit Radom-Aizik
E-mail(s) saizik@uci.edu
Phone 949-824-2584
Organization name University of California, Irvine
Department Pediatrics
Lab Pediatric Exercise and Genomics Research Center
Street address 101 Academy
City Irvine
State/province CA
ZIP/Postal code 92617
Country USA
 
Platform ID GPL570
Series (1)
GSE8668 Effects of exercise on gene expression in human neutrophils
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE86362
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE GC-RMA

Data table
ID_REF VALUE
1007_s_at 8.471309
1053_at 67.27031
117_at 933.58417
121_at 12.997316
1255_g_at 4.1401825
1294_at 158.72302
1316_at 9.970598
1320_at 5.831109
1405_i_at 4576.2925
1431_at 7.55517
1438_at 4.4095216
1487_at 55.842213
1494_f_at 5.223091
1552256_a_at 7.976429
1552257_a_at 83.32647
1552258_at 14.897036
1552261_at 7.6727486
1552263_at 475.5759
1552264_a_at 1294.2205
1552266_at 8.229683

Total number of rows: 54675

Table truncated, full table size 1087 Kbytes.




Supplementary file Size Download File type/resource
GSM215000.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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