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Sample GSM1576831 Query DataSets for GSM1576831
Status Public on Aug 01, 2015
Title Skeletal Muscle Sample 8 (experiment, low-force)
Sample type RNA
 
Source name skeletal muscle, experiment, low-force
Organism Homo sapiens
Characteristics tissue: skeletal muscle
gender: male
treatment: experiment, low-force
Treatment protocol Subjects completed a single unilateral session of low or high force exercise 3 hours before a muscle biopsy or subjects unilaterally trained one limb with exercise.
Extracted molecule total RNA
Extraction protocol Following harvest, muscle biopsy samples were immediately placed In RNALater (Ambion) and stored at -80 C until further use. Total RNA was extracted using TRIzol solution (Invitrogen) according to the manufacturer’s instructions. 50 ng of RNA was converted to SPIA amplified cDNA using the WT-Ovation Pico RNA Amplification System, v1 (NuGEN Technologies, San Carlos, CA, Cat. #3300) according to the manufacturer’s recommended protocol. The amplified SPIA cDNA product was purified through a QIAGEN MinElute Reaction Cleanup column (QIAGEN Cat #28204) according to modifications from NuGEN. Four μg of SPIA amplified DNA were used to generate ST-cDNA using the WT-Ovation Exon Module v1 (NuGEN Technologies, Cat #2000) and again cleaned up with the Qiagen column as above.
Label Biotin
Label protocol 5μg of this product were fragmented (average fragment size = 85 bases) and biotin labeled using the NuGEN FL-Ovation cDNA Biotin Module, v2 (NuGEN Technologies, Cat. #4200) per the manufacturer’s recommended protocol.
 
Hybridization protocol Biotin-labeled cDNA was mixed with Affymetrix eukaryotic hybridization buffer and placed onto Affymetrix Human Exon 1.0 ST arrays. Hybridizations were performed by the DNA Core Facility at the University of Iowa.
Scan protocol Arrays were scanned with the Affymetrix Model 3000 scanner with 7G upgrade and data were collected using the GeneChip operating software (GCOS) v1.4.
Description RMA expression value derived from Partek Genomic Suites
Data processing Arrays were normalized using a Robust Multi-array Average (RMA) and transformed into a log2 hybridization signal using Partek Genomic Suites (v6.6 Copyright © 2013 Partek Inc., St. Louis, MO, USA).
 
Submission date Jan 05, 2015
Last update date Aug 01, 2015
Contact name Richard Shields
Organization name The University of Iowa
Street address 1-252 Medical Education Building
City Iowa City
ZIP/Postal code 52242
Country USA
 
Platform ID GPL5175
Series (1)
GSE64683 Influence of low and high force muscle activity on paralyzed muscle gene expression

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
2315554 5.39482
2315633 5.50814
2315674 5.54892
2315739 5.62108
2315894 7.31279
2315918 3.96774
2315951 5.31535
2316218 4.37264
2316245 5.08971
2316379 6.06969
2316558 7.77339
2316605 5.15153
2316746 5.69097
2316905 4.20437
2316953 5.06003
2317246 5.11644
2317317 5.2718
2317434 6.67062
2317472 5.21008
2317512 5.0036

Total number of rows: 22011

Table truncated, full table size 341 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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