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Status |
Public on Mar 15, 2010 |
Title |
HSC sample 1 |
Sample type |
RNA |
|
|
Source name |
Lin(CD3e; CD4, CD8a, CD19, CD45R, CD127; Gr1, TER119)- CD117+ Sca1+
|
Organism |
Mus musculus |
Characteristics |
genetic background: C57Bl6 cell type: HSC
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction following manufacturer's protocol.
|
Label |
Biotin
|
Label protocol |
10 to 50 nanograms of total RNA was amplified and processed to produce biotinylated cDNA targets using two round of in vitro RNA synthesis
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|
|
Hybridization protocol |
3.75 micrograms of biotinylated material was hybridized according to the standard Affymetrix protocol.
|
Scan protocol |
Standard Affymetrix protocol
|
Description |
purified Lineage- CD117+ Sca1+ cells form 8 week old female mice
|
Data processing |
RMA background correction and quantile normalization done with the GenePattern ExpressionFileCreator module (http://www.broad.mit.edu/cancer/software/genepattern/) which uses the Bioconductor implementation of RMA (http://www.bioconductor.org/). This function computes the Robust Multichip Average expression measure described in Irizarry et al Biostatistics (2003).
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|
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Submission date |
Feb 17, 2010 |
Last update date |
Feb 17, 2010 |
Contact name |
Amit Sinha |
E-mail(s) |
[email protected]
|
Phone |
617-582-7579
|
Organization name |
Dana-Farber Cancer Institute
|
Department |
Pediatric Oncology
|
Lab |
Armstrong Lab
|
Street address |
44 Binney St
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02135 |
Country |
USA |
|
|
Platform ID |
GPL8321 |
Series (1) |
GSE20377 |
Activation or maintenance of a leukemia stem cell self-renewal pathway in downstream myeloid cells |
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