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Status |
Public on Jun 07, 2011 |
Title |
HNG2 |
Sample type |
RNA |
|
|
Source name |
HNG2
|
Organism |
Mus musculus |
Characteristics |
cell type: Hepatic progenitor cells strain: STOCK Tg(Nanog-GFP, Puro)1 Yam development stage: E13.5 129/Sv x C57BL/6
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was prepared using the ISOGEN kit (Nippon gene co, Tokyo Japan) following the manufacturer's recommendations. All RNA wwere quantified using a NanoDrop-1000 spectrophotometer.
|
Label |
Cy3
|
Label protocol |
Agilent one-color Low RNA Fluorecent Liner Amplification kit labeling protocol. Cyanine-3 (Cy3) labeled cRNA was prepared from 0.25 ug RNA according to the manufacturer's instructions. Dye incorporation and cRNA yield were checked with the NanoDrop Spectrophotometer.
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|
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Hybridization protocol |
Agilent one-color gene expression hyb/wash protocol. 1.65 ug of Cy3 labeled RNA was hybridized to Agilent Whole Mouse Genome microarrays (4 x 44K: GPL4134) at 60C for 17 hours and subsequently washed according to the Agilent standard hybridization protocol.
|
Scan protocol |
Microarray slides were scanned in an Agilent Technologies G2539A Microarray Scanner at 5 micron resolution. Images were quantified using Agilent Feature Extraction software version 9.5.3.1
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Data processing |
Agilent Feature Extraction software; gProcessedSignal; processed Cy3 Signal
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Submission date |
Jun 03, 2011 |
Last update date |
Jun 09, 2011 |
Contact name |
Takafusa Hikichi |
E-mail(s) |
thikichi@ri.ncgm.go.jp
|
Organization name |
National Center for Global Health and Medicine
|
Street address |
1-21-1 Toyama, Shinjuku-ku
|
City |
Tokyo |
ZIP/Postal code |
162-8655 |
Country |
Japan |
|
|
Platform ID |
GPL4134 |
Series (2) |
GSE29730 |
Unsupervised hierarchical clustering of iHPCs induced by 9 or 10 TFs |
GSE29875 |
Systematic identification of transcription factors capable of inducing cell-type-specific transcriptional profiles |
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