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Status |
Public on Jul 31, 2010 |
Title |
Gastrocnemius Muscle_WT_rep1 |
Sample type |
RNA |
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Source name |
Gastrocnemius, WT, 2 months old
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Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J genotype: wild type gender: male age: 2 months tissue: Gastrocnemius muscle
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Growth protocol |
All mice were maintained in the institute animal facility following the IACUC guidelines.
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions followed by further purification on a silica-gel-based membrane (RNeasy-Mini; Qiagen, Valencia, CA).
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Label |
Biotin
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Label protocol |
The Ovation™ Biotin RNA Amplification and Labeling System (NuGen Technologies, Inc., San Carlos, CA) was used to prepare amplified, biotin-labeled cDNA from 25 ng of total RNA following manufacturer’s instructions.
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Hybridization protocol |
For each array, 2.2 µg of fragmented and labeled cDNA was hybridized onto 430 2.0 GeneChips® (Affymetrix Inc., USA), for 16 hours at 45ºC followed by washing and staining of microarrays in a Fluidics Station 450 (Affymetrix Inc., USA).
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Scan protocol |
GeneChips were scanned in a GeneChip Scanner 3000 (Affymetrix Inc., USA).
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Description |
Gene expression data from skeletal muscle of two-month-old WT mouse. 66WT Skeletal Muscle
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Data processing |
CEL files were generated from DAT files using GeneChip® Operating Software (GCOS) software (Affymetrix Inc., USA) and probe set signals were generated using the RMA algorithm in ArrayAssist 3.4 (Stratagene). Differential gene expression was determined by pair-wise comparisons.
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Submission date |
Jun 04, 2009 |
Last update date |
Dec 21, 2009 |
Contact name |
Paul T Martin |
E-mail(s) |
[email protected]
|
Organization name |
Columbus Children's Research Institute
|
Street address |
700 Children's Drive
|
City |
Columbus |
State/province |
OH |
ZIP/Postal code |
43205 |
Country |
USA |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE16438 |
Array profiling of dystrophin-deficient mice with a secondary glycosylation defect |
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