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Status |
Public on Jan 08, 2021 |
Title |
HEK239flpGR_siNON_dex_6h_rep1 |
Sample type |
RNA |
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|
Source name |
Isogenic HEK293 cells, wild-type GR, siNON treated, 72h, dex treated, 6h
|
Organism |
Homo sapiens |
Characteristics |
cell line: HEK293 cell type: human embryonal kidney cell line stably expressing: wild-type GR sirna treatment: Dharmacon On-TARGETplus SMARTpool for nontargeting pool sirna concentration: 40 nM time for sirna: 72 h ligand treatment: dexamethasone ligand concentration: 100 nM time for ligand: 6 h
|
Treatment protocol |
siUBC9 or siNON in 40 nM final concentration were added with Lipofectamine RNAiMAX to 6-well plates and incubated for 20 min RT. Subsequently, 300,000 isogenic HEK293 cells were seeded at each 6-well plates and allowed to grow in steroid-depleted medium (2.5% charcoal stripped FBS in DMEM) 72 h. The cells were treated with or without 100 nM of dexamethasone for 6 h prior extraction of RNA.
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Growth protocol |
Isogenic HEK293 cells were grown in Dulbecco's Modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum, 25 U/ml penicillin and 25 µg/ml streptomycin, and 100 µg hygromycin-B, and kept at 37 °C in a humidified 95% air/ 5% CO2.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using TriPure (Roche Diagnostics GmbH, Mannheim, Germany) according to manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmk kit for Illumina arrays.
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|
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Hybridization protocol |
Standard Illumina hybridization protocol.
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Scan protocol |
Standard Illumina scanning protocol. Arrays were scanned by Illumina BeadArray Reader.
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Description |
NON_4 HEK293flpGR cells were created by using the Flp-In System (Invitrogen).
|
Data processing |
Obtained data was normalized using VST transformation and RSN normalization used as standard approach for Illumina arrays with the R/lumi package.
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Submission date |
Dec 19, 2014 |
Last update date |
Jan 08, 2021 |
Contact name |
Ville Paakinaho |
E-mail(s) |
[email protected]
|
Organization name |
University of Eastern Finland
|
Department |
School of Medicine
|
Lab |
Biomedicine
|
Street address |
Yliopistonranta 8
|
City |
Kuopio |
ZIP/Postal code |
70210 |
Country |
Finland |
|
|
Platform ID |
GPL10558 |
Series (2) |
GSE64372 |
SUMOylation regulates the protein network and chromatin accessibility at glucocorticoid receptor-binding sites [array] |
GSE64373 |
SUMOylation regulates the protein network and chromatin accessibility at glucocorticoid receptor-binding sites |
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