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Status |
Public on Aug 01, 2013 |
Title |
5-LSK_Tet2_Ezh2_DKO_MDS/MPN |
Sample type |
RNA |
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Source name |
Tet2KD/KDEzh2-/- MDS/MPN LSK from BM
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 cell type: LSK cells purified from: BM genotype/variation: Tet2KD/KDEzh2-/- MDS/MPN
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
Cy3
|
Label protocol |
250 ng of total RNA was mixed with spike-in controls using an Agilent One Color Spike Mix Kit (Agilent Technologies), amplified and labeled with Cyanine 3 using a Quick Amp Labeling Kit (Agilent Technologies) according to the manufacturer's instructions, which generated single-color labeled cRNA.
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Hybridization protocol |
1,650 ng of the labeled cRNA was hybridized to Agilent Whole Mouse Genome 4x44k array Ver.2, Design ID: 028005. The process of hybridization and washing was performed using a Hi-RPM Gene Expression Hybridization Kit (Large) (Agilent Technologies) and a Gene Expression Wash Pack (Agilent Technologies) respectively.
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Scan protocol |
GeneChips were scanned using a DNA microarray scanner (Agilent Technologies)
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Description |
Gene expression data of LSK from Tet2KD/KDEzh2-/- mice that developed myelodysplastic/myeloproliferative neoplasm (MDS/MPN)
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Data processing |
standard Agilent protocol
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Submission date |
Dec 02, 2012 |
Last update date |
Aug 01, 2013 |
Contact name |
ATSUSHI IWAMA |
E-mail(s) |
[email protected]
|
Phone |
81-43-226-2187
|
Fax |
81-43-226-2191
|
Organization name |
Graduate School of Medicine, Chiba University
|
Department |
Department of Cellular and Molecular Medicine
|
Street address |
1-8-1 Inohana, Chuo-ku
|
City |
Chiba |
ZIP/Postal code |
260-8670 |
Country |
Japan |
|
|
Platform ID |
GPL13912 |
Series (1) |
GSE42666 |
Expression data from Tet2-hypomorph (knockdown) and/or Ezh2-null Lineage-Sca-1+c-Kit+ (LSK) cells and granulocyte-macrophage progenitors (GMPs) |
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