|
Status |
Public on Aug 11, 2010 |
Title |
macrophage_rIAPP15uM_12h_rep1 |
Sample type |
RNA |
|
|
Source name |
mouse bone marrow-derived macrophage
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 media: DMEM with 10% FBS treatment: rat IAPP cell type: bone marrow-derived macrophage
|
Treatment protocol |
Cells were treated with 15 mM rat or human IAPP dissolved in media, and incubated for 12 hours at 37 degrees C.
|
Growth protocol |
BMDMs were propagated from bone marrow in complete DMEM containing 15% L929-conditioned media for 7 days. Cells were seeded in 24-well plates and starved of L929-containing media for 12 hours prior to the experiment.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Buffer RLT provided in a QIAGEN RNeasy Plus mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with an Agilent Bioanalyser.
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
Rat IAPP, Replicate 1
|
Data processing |
The data were normalized by the rank-invariant method in Bead Studio
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|
|
Submission date |
Aug 10, 2010 |
Last update date |
Aug 10, 2010 |
Contact name |
Clara Westwell-Roper |
E-mail(s) |
[email protected]
|
Phone |
604-875-3792
|
Organization name |
Child and Family Research Institute, University of British Columbia
|
Department |
Pathology and Laboratory Medicine
|
Lab |
Dr. C. Bruce Verchere
|
Street address |
950 West 28th Ave
|
City |
Vancouver |
State/province |
BC |
ZIP/Postal code |
V5Z 4H4 |
Country |
Canada |
|
|
Platform ID |
GPL6885 |
Series (1) |
GSE23534 |
Effect of hIAPP aggregation on gene expression by mouse bone marrow-derived macrophages after 12 hours |
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