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Status |
Public on Sep 04, 2013 |
Title |
CD45.2+LSK_RUNX1S291fs |
Sample type |
RNA |
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Source name |
Bone marrow CD45.2+LSK cells, RUNX1S291fs, replicate 1
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Organism |
Mus musculus |
Characteristics |
tissue: bone marrow LSKs disease stage: normal, pre-MDS genotype: RUNX1S291fs cd45: CD45.2 cell type: Bone marrow CD45.2+LSK cells genetic background: C57BL/6
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Treatment protocol |
Freshly isolated bone marrow cells were stained by appropriate antibodies, and then sorted on FACSAriaII (BD).
|
Extracted molecule |
total RNA |
Extraction protocol |
RNeasy Plus Mini Kit (Qiagen) extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
Cy3
|
Label protocol |
20 ng of total RNA was mixed with spike-in controls using an Agilent One Color Spike Mix Kit (Agilent), amplified and labeled with Cyanine 3 using a Low Input Quick Amp Labeling Kit (Agilent) according to the manufacturer's instructions, which generated single-color labeled cRNA.
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Hybridization protocol |
600 ng of the labeled cRNA was hybridized to Agilent SurePrint G3 Mouse GE 8x60K Microarray. The process of hybridization and washing was performed using a Hi-RPM Gene Expression Hybridization Kit (Large) (Agilent) and a Gene Expression Wash Pack (Agilent), respectively.
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Scan protocol |
GeneChips were scanned using a DNA microarray scanner (Agilent Technologies)
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Description |
Gene expression at 4 months post-transplantation in RUNX1S291fs LSK cells
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Data processing |
Standard Agilent protocol
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Submission date |
Sep 03, 2013 |
Last update date |
Sep 05, 2013 |
Contact name |
Goro Sashida |
Organization name |
Kumamoto University
|
Department |
IRCMS
|
Lab |
Transcriptional Regulation in Leukemogenesis
|
Street address |
2-2-1 Honjo, Chuo-ku
|
City |
Kumamoto |
State/province |
Kumamoto |
ZIP/Postal code |
860-0811 |
Country |
Japan |
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Platform ID |
GPL10787 |
Series (1) |
GSE50537 |
Expression data from RUNX1S291fs-mutant and/or Ezh2 conditional knockout Lineage-c-Kit+Sca-1+ (LSK) cells |
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