|
Status |
Public on Feb 15, 2018 |
Title |
RootHair_WT_rep3 |
Sample type |
RNA |
|
|
Source name |
Root hair cells
|
Organism |
Arabidopsis thaliana |
Characteristics |
genotype: WT gfp flourescent: FACS using pEXPA7:NLS-GFP
|
Treatment protocol |
Seedling roots, 5 days after germination
|
Growth protocol |
On MS media for 5 days
|
Extracted molecule |
total RNA |
Extraction protocol |
Plotoplasts were isolated from root tissues and GFP-expressing cells were collected by FACS methods. Total RNA from plotoplasts was purified by Qiagen Rneasy kit.
|
Label |
biotin
|
Label protocol |
Affy two-cycle labeling (raw 21-26) and one-cycle (everything else) labeling protocol
|
|
|
Hybridization protocol |
Standard Operating Procedure performed at the Duke Microarray Facility
|
Scan protocol |
Standard Operating Procedure performed at the Duke Microarray Facility
|
Description |
Gene expression data from root hair cells isolated by FACS using pEXPA7:NLS-GFP
|
Data processing |
The gcRMA implementation in the Bioconductor and R software packages were used for background correction, quantile normalization and expression-estimate computation.
|
|
|
Submission date |
Sep 15, 2017 |
Last update date |
Feb 15, 2018 |
Contact name |
Michitaro Shibata |
E-mail(s) |
michitaro.shibata@riken.jp
|
Organization name |
RIKEN
|
Department |
CSRS
|
Lab |
Cell function research team
|
Street address |
1-7-22 Suehirocho Tsurumi
|
City |
Yokohama |
State/province |
Kanagawa |
ZIP/Postal code |
230-0045 |
Country |
Japan |
|
|
Platform ID |
GPL198 |
Series (1) |
GSE103917 |
Root hair specific transcriptome analysis of gain-of-function and loss-of-function of GTL1 and DF1 |
|