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Status |
Public on Sep 08, 2014 |
Title |
LSK-Control-K1603 |
Sample type |
RNA |
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|
Source name |
Wild type LSKs
|
Organism |
Mus musculus |
Characteristics |
strain background: C57/BL6 genotype/variation: Dot1 wt/wt x Mx-Cre; wild type cell type: Sorted BM cells cell subtype: Lineage negative Sca-1 positive Kit positive (LSK) cells
|
Treatment protocol |
Cells were sorted on the basis of surface markers for LSKs and GMPs using standard protocols prior to RNA preparation.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA and Qiagen RNeasy micro kit was performed according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 100 ng total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
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|
|
Hybridization protocol |
According to manufacturer's instructions (Affymetrix)
|
Scan protocol |
According to manufacturer's instructions (Affymetrix)
|
Description |
Wild type LSKs
|
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 |
Jan 29, 2014 |
Last update date |
Sep 08, 2014 |
Contact name |
Scott Armstrong |
Organization name |
Memorial Sloan-Kettering Cancer Center
|
Street address |
1275 York Avenue
|
City |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
|
|
Platform ID |
GPL1261 |
Series (2) |
GSE54498 |
Effect of Dot1l deletion on LSKs and GMPs |
GSE54500 |
Role of H3K79 methylation states in HOX gene expression and leukemogenesis |
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