NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM7439160 Query DataSets for GSM7439160
Status Public on Jun 06, 2023
Title UKK2_hiPSC_Buspirone_Day1_R2
Sample type RNA
 
Source name IMR90 hiPSC cells
Organism Homo sapiens
Characteristics gender: female
state: proliferating state
agent: Buspirone
time point: Day1
Treatment protocol Cells were incubated (5 % CO2, 37 °C) with the test compounds at different concentrations and a DMSO concentration of 0.1 % or 0.5 %.
Growth protocol Cells were differentiated in RPMI 1640 GlutaMAX™ medium (Thermo Fisher Scientific, Germany) plus B-27™ Supplement, minus insulin (Thermo Fisher Scientific, Germany) supplemented with 10 µM Wnt activator small molecule CHIR99021 (R&D Systems, Minneapolis, USA).
Extracted molecule total RNA
Extraction protocol The cells were homogenised with TRIzol lysis reagent (Thermo Fisher Scientific, Germany), and the total RNA was extracted and purified using the RNeasy Mini Kit (Qiagen, Germany) according to the manufacturer’s instructions.
Label biotin
Label protocol The samples were amplified and labelled with biotin using GeneChip 3′ IVT Express Kit per the manufacturer’s instructions (Affymetrix, High Wycombe, UK).
 
Hybridization protocol The samples were purified using magnetic beads and fragmented. 12,5 μg of fragmented RNA samples were hybridized on Affymetrix Human Genome U133 Plus 2.0 arrays (Affymetrix, Santa Clara, CA, USA). The microarray hybridization step was performed in an Affymetrix GeneChip Hybridization Oven-645 for 16 h at 45 °C and 60 rpm. Washing and staining of the hybridized arrays was completed using the GeneChip HWS Kit (Affymetrix, High Wycombe, United Kingdom) and Affymetrix GeneChip Fluidics Station-450.
Scan protocol Stained arrays were scanned with Affymetrix Gene-Chip Scanner-3000-7G and evaluated for quality control with Affymetrix GCOS software
Data processing All analyses were conducted using the statistical software R, version 4.2.2. Pre-processing of the data consists of the three steps background correction, normalization, and summarization, using the frozen robust multi-array average (fRMA) algorithm. This yields expression values for 54675 probe sets. The R-packages affy, frma and hgu133plus2frmavecs were used.
 
Submission date Jun 01, 2023
Last update date Jun 06, 2023
Contact name Agapios Sachinidis
E-mail(s) a.sachinidis@uni-koeln.de
Phone +492214787373
Organization name University of Cologne
Department Institute of Neurophysiology
Street address Robert-Kochstr. 39
City Cologne
State/province NRW
ZIP/Postal code 50931
Country Germany
 
Platform ID GPL570
Series (2)
GSE233924 Identification of cardiac developmental toxicants in differentiated human induced pluripotent stem cells [Toxicants]
GSE233926 Identification of cardiac developmental toxicants in differentiated human induced pluripotent stem cells

Data table header descriptions
ID_REF
VALUE Log2-transformed expression values

Data table
ID_REF VALUE
1007_s_at 8.802836519
1053_at 9.11134107
117_at 5.284218922
121_at 7.466213012
1255_g_at 4.82294634
1294_at 5.585713912
1316_at 5.755187693
1320_at 4.584396496
1405_i_at 3.746334368
1431_at 3.503585919
1438_at 5.948692349
1487_at 7.537660376
1494_f_at 5.289014845
1552256_a_at 8.182298453
1552257_a_at 7.972377281
1552258_at 3.706720086
1552261_at 4.824923672
1552263_at 7.431774308
1552264_a_at 7.816203196
1552266_at 3.305407787

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM7439160_23.a_6.12.21_Anna_HG-U133_Plus_2_.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap