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Status |
Public on May 10, 2012 |
Title |
VE-Cadherin+/CD45-(P3) cells from Tie-2 Embryo proper(Emb) rep2 |
Sample type |
RNA |
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Source name |
Mouse Embryos (E11.5); Tie-2-Etv2(Etv2 Tg turned ON by Tie-2 Cre Tg) Emb
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Organism |
Mus musculus |
Characteristics |
cell type: VE-Cadherin+/CD45-(P3) strain: mixed (B6/CBA and others) genotype/variation: Tie-2-Etv2 tissue: embryo proper
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Biomaterial provider |
Knock-in and Tg mice crossed at CDB RIKEN
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Treatment protocol |
FACS sort only, no treatment afterwards
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Growth protocol |
FACS sort only, no treatment afterwards
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Extracted molecule |
total RNA |
Extraction protocol |
We used Qiagen RNA microelute Kit.
|
Label |
Cy3
|
Label protocol |
We used Agilent Low Input Quick Amp Labeling Kit, and followed manufacturer's protocol. http://www.chem.agilent.com/Library/usermanuals/Public/G4140-90040_GeneExpression_One-color_v6.5.pdf
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Hybridization protocol |
We used Agilent Hybridization Oven, and followed manufacturer's protocol. http://www.chem.agilent.com/Library/usermanuals/Public/G4140-90040_GeneExpression_One-color_v6.5.pdf
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Scan protocol |
We used Agilent Microarray Scanner, and followed manufacturer's protocol. http://www.chem.agilent.com/Library/usermanuals/Public/G4140-90040_GeneExpression_One-color_v6.5.pdf
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Data processing |
We used Agilent Feature Extraction 10.7 for quantification, and GeneSpring GX11.5.1 for data analysis. 1. Data Transformation: Set measurements less than 1 to 1 2. Per Chip: Normalize to 75 percentile 3. Per Gene: Normalize to median
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Submission date |
Mar 14, 2012 |
Last update date |
May 10, 2012 |
Contact name |
Hiroshi Kataoka |
Organization name |
Riken Center for Developmental Biology
|
Department |
Stem Cell Biology
|
Street address |
2-2-3 Minatojima-minamimachi, Chuo-ku
|
City |
Kobe |
State/province |
Hyogo |
ZIP/Postal code |
650-0047 |
Country |
Japan |
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Platform ID |
GPL10787 |
Series (1) |
GSE36516 |
Gene expression profiling in Tie-2-Etv2 endothelial and/or hematopoietic precursors |
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