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Sample GSM8023460 Query DataSets for GSM8023460
Status Public on Sep 23, 2024
Title MSC_NSC_2_3 h (transcriptome)
Sample type RNA
 
Source name human bone marrow-derived MSCs , 3h
Organism Homo sapiens
Characteristics cell type: human bone marrow-derived MSCs
timepoint: 3h
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 50.0934621428571
A_22_P00006924 6.31055144642857
A_23_P168868 21022.1294125
A_23_P303423 138.444567857143
A_22_P00017229 8.57094980357143
A_23_P66260 366.905369642857
A_21_P0014627 7.74412191071429
A_22_P00023979 5.69953680357143
A_23_P49646 2151.56112678571
A_33_P3224680 427.258991071429
A_23_P88331 2389.15245
A_33_P3360142 6.99965269107143
A_22_P00010977 9.865816625
A_23_P78438 10692.2638821429
A_22_P00019001 13.1674471428571
A_33_P3387781 12.3259751785714
A_21_P0009323 83.5429160714286
A_33_P3330546 2690.643025
A_33_P3269149 110.551171785714
A_22_P00004184 6.63913289285714

Total number of rows: 50038

Table truncated, full table size 1466 Kbytes.




Supplementary file Size Download File type/resource
GSM8023460_US11153896_257236346361_S01_GE1_1200_Jun14_1_1.txt.gz 3.0 Mb (ftp)(http) TXT

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