|
Status |
Public on May 22, 2024 |
Title |
siNFAT5 under High Na condition |
Sample type |
RNA |
|
|
Source name |
HeLa cells
|
Organism |
Homo sapiens |
Characteristics |
treatment: treatment: siNFAT5
|
Treatment protocol |
HeLa cells were transfected with siControl, siNFAT5 and siHES1 using lipofectamine RNAiMax.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA were extracted using Isogen (Wako, Cat#319-90211).
|
Label |
biotin
|
Label protocol |
Biotinylated cDNA was prepared from total RNA using GeneChip WT PLUS Reagent Kit (Affymetrix) following the manufacturer’s instructions.
|
|
|
Hybridization protocol |
single stranded cDNA was hybridized for 16 hr at 45˚C on Clariom S Human Array Thermo Fisher Scientific).
|
Scan protocol |
Arrays were washed and stained in the GeneChip Fluidics Station 450 (Affymetrix) and were scanned using GeneChip Scanner 3000 7G.
|
Description |
RMA expression value derived from Affymetrix Expression Console Software.
|
Data processing |
Gene expression data were analyzed with Affymetrix Expression Console Software 1.4.1 offered SST-RMA using Affymetrix default analysis settings.
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|
|
Submission date |
May 16, 2024 |
Last update date |
May 22, 2024 |
Contact name |
Hiroki Ryuno |
Organization name |
The University of Tokyo
|
Department |
Graduate School of Pharmaceutical Sciences
|
Lab |
Laboratory of Cell Signaling
|
Street address |
7-3-1
|
City |
Hongo, Bunkyo-ku |
State/province |
Tokyo |
ZIP/Postal code |
113-0033 |
Country |
Japan |
|
|
Platform ID |
GPL23159 |
Series (1) |
GSE267676 |
Gene expression data from HeLa cells under high salt condition |
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