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Sample GSM8023464 Query DataSets for GSM8023464
Status Public on Sep 23, 2024
Title MSC_NSC_2_24 h (transcriptome)
Sample type RNA
 
Source name human bone marrow-derived MSCs , 24h
Organism Homo sapiens
Characteristics cell type: human bone marrow-derived MSCs
timepoint: 24h
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 40.3821925535714
A_22_P00006924 8.10785059628572
A_23_P168868 16480.8210196429
A_23_P303423 51.3897794642857
A_22_P00017229 10.8902183928571
A_23_P66260 121.296075339286
A_21_P0014627 13.8208544642857
A_22_P00023979 8.78566278928571
A_23_P49646 1760.39396607143
A_33_P3224680 252.702826785714
A_23_P88331 21.5972310714286
A_33_P3360142 6.61990505357143
A_22_P00010977 7.8673035
A_23_P78438 9084.81446607143
A_22_P00019001 11.7114117142857
A_33_P3387781 14.5369667321429
A_21_P0009323 105.997319642857
A_33_P3330546 3639.73772321429
A_33_P3269149 155.507973214286
A_22_P00004184 11.2824344392857

Total number of rows: 50038

Table truncated, full table size 1466 Kbytes.




Supplementary file Size Download File type/resource
GSM8023464_US11153896_257236346361_S01_GE1_1200_Jun14_2_1.txt.gz 3.1 Mb (ftp)(http) TXT

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