|
Status |
Public on May 10, 2012 |
Title |
KSL cells from Vav-Etv2 bone marrow rep1 |
Sample type |
RNA |
|
|
Source name |
KSL cells from 6 weeks Vav-Etv2(Etv2 Tg turned ON by Vav-iCre Tg)
|
Organism |
Mus musculus |
Characteristics |
cell type: KSL age: 6 weeks strain: mixed (B6/CBA and others) genotype/variation: Vav-Etv2 tissue: bone marrow
|
Biomaterial provider |
Knock-in and Tg mice crossed at CDB RIKEN
|
Treatment protocol |
FACS sort only, no treatment afterwards
|
Growth protocol |
FACS sort only, no treatment afterwards
|
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
|
|
|
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
|
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
|
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
|
|
|
Submission date |
Mar 23, 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 |
|
|
Platform ID |
GPL10787 |
Series (1) |
GSE36731 |
Gene expression profiling in Vav-Etv2 KSL and Granulocyte hematopoietic cells |
|