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Status |
Public on Apr 13, 2018 |
Title |
Weight_stable [ID116_019F] |
Sample type |
RNA |
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|
Source name |
Subcutaneous adipose tissue
|
Organism |
Homo sapiens |
Characteristics |
weight status: Weight_stable tissue: White adipose tissue genotype: female age: 31
|
Treatment protocol |
Biopsies from the abdominal subcutaneous adipose tissue depot were obtained by aspiration needle biopsly. Samples were immediately washed in NacCl (9 mg/ml) and thereafter frozen in liquid nitrogen and kept at -70C for subsequent RNA preparation.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated using the RNeasy kit (cat no. 217004, Qiagen) according to the manufacturer’s instructions.
|
Label |
biotin
|
Label protocol |
The WT Plus Kit was used to generate amplified and biotinylated sense-strand DNA targets from total RNA (Thermo Fisher).
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|
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Hybridization protocol |
A total of 5.5 µg of fragmented and biotinylated sense-strand DNA target were hybridized to the arrays in a GeneChip Hybridization Oven 645 for 16-18h at 45°C.
|
Scan protocol |
The arrays were washed and stained in the Gene Chip Fluidics Station 450 followed by scanning in an Affymetrix Gene Chip Scanner 7.
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Data processing |
CEL files were analyzed in Affymetrix Expression Console (v. 1.4.1) using the SST-RMA method. Microarray gene expression (log2-values) was analyzed in Qlucore (www.qlucore.com).
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Submission date |
Apr 12, 2018 |
Last update date |
Apr 13, 2018 |
Contact name |
Ingrid Dahlman |
E-mail(s) |
[email protected]
|
Organization name |
Karolinska
|
Street address |
Karolinska Huddinge
|
City |
Stockholm |
ZIP/Postal code |
14186 |
Country |
Sweden |
|
|
Platform ID |
GPL23126 |
Series (1) |
GSE113080 |
Altered adipose lipid mobilization predicts long-term weight gain and impaired glucose metabolism |
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