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Sample GSM8023462 Query DataSets for GSM8023462
Status Public on Sep 23, 2024
Title MSC_NSC_2_9 h (transcriptome)
Sample type RNA
 
Source name human bone marrow-derived MSCs , 9h
Organism Homo sapiens
Characteristics cell type: human bone marrow-derived MSCs
timepoint: 9h
replicate: R2
treatment: neurogenic differentiation medium
Treatment protocol Time-course cell samples were collected at 0, 3, 6, 9, 12, 24 and 48 h after addition of a standard commercial neurogenic differentiation medium (C-28015, PromoCell).
Growth protocol Cells were seeded at a density of 100.000 per 25 cm2 flask (coated with fibronectin), grown with Mesenchymal Stem cell Growth Medium (PromoCell) and expanded for 1-2 passages before induction of the trans-differentiation.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared using the miRNeasy Mini Kit (Qiagen, Hilden, Germany) following the manufacturer's recommendations.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeling of cRNA was performed following the instructions from Low Input Quick Amp Labeling Kit (One-Color) (Agilent Technologies, Santa Clara, CA, USA). The cRNA samples were using RNeasy Mini Kit (Qiagen, Hilden, Germany). Resulting cRNA concentrations were determined using a NanoDrop™ 2000c Spectrophotometer (Thermo Fisher Scientific Inc., Waltham, MA, USA).
 
Hybridization protocol The labeled cRNA samples were hybridized to Human SurePrint G3 Gene Expression Microarrays (V3, G4851C) from Agilent Technologies following the inctructions from the Gene Expression Hybridization Kit (Agilent Technologies)
Scan protocol The microarray slides were scanned with a resolution of 3 μm.
Data processing Raw data was extracted using Feature Extraction software (Agilent Technologies, Santa Clara, CA, USA). Raw microarray data were extracted and concatenated into one matrix using python (v 3.7) with numpy (v 1.16.4).
 
Submission date Jan 18, 2024
Last update date Sep 23, 2024
Contact name Annika Engel
E-mail(s) [email protected]
Organization name Saarland University
Department Center for Bioinformatics
Lab Chair for Clinical Bioinformatics
Street address Campus E2 1
City Saarbrücken
State/province Saarland
ZIP/Postal code 66123
Country Germany
 
Platform ID GPL21185
Series (2)
GSE253566 Paving the way to a neural fate - RNA signatures in naive and trans-differentiating Mesenchymal Stem Cells - transcriptome data
GSE253567 Paving the way to a neural fate - RNA signatures in naive and trans-differentiating Mesenchymal Stem Cells

Data table header descriptions
ID_REF
VALUE Quantile normalization, log2 transformation using R (v 3.5.1) with data.table (v 1.12.0) and Bioconductor-preprocesscore (v 1.46.0).

Data table
ID_REF VALUE
A_22_P00013941 41.5892823214286
A_22_P00006924 4.66082696428572
A_23_P168868 23669.6991982143
A_23_P303423 59.7947698214286
A_22_P00017229 10.9152169857143
A_23_P66260 178.3458567625
A_21_P0014627 6.09844689285714
A_22_P00023979 7.86111479821429
A_23_P49646 2130.03834107143
A_33_P3224680 267.614806410714
A_23_P88331 2359.39677303571
A_33_P3360142 5.56272826785714
A_22_P00010977 11.6128215517857
A_23_P78438 10692.2638821429
A_22_P00019001 10.4237199821429
A_33_P3387781 15.7122361089286
A_21_P0009323 103.5702125
A_33_P3330546 3435.42205357143
A_33_P3269149 125.312942857143
A_22_P00004184 27.3998351785714

Total number of rows: 50038

Table truncated, full table size 1466 Kbytes.




Supplementary file Size Download File type/resource
GSM8023462_US11153896_257236346361_S01_GE1_1200_Jun14_1_3.txt.gz 3.0 Mb (ftp)(http) TXT

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