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Sample GSM3526890 Query DataSets for GSM3526890
Status Public on Apr 23, 2019
Title Fasting 3999844010_J
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: 91/78
viability: alive
condition: NPC-N
gender: K
Treatment protocol Fasting conditions - cells were cultured in medium with lipoprotein deprived serum. LDL+LPDS - cells were cultured in medium with LPDS and then supplemented with LDL source.
Growth protocol All cell lines were cultured in DMEM (Thermo Fisher Scientific Inc.) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin solution (Sigma-Aldrich Co. LLC., St. Louis, USA) in a humidified atmosphere containing 5% CO2 at 37°C. Cells were harvested after trypsinization when the culture was confluent, immediately immersed in RNA Later (Qiagen), and stored at -70°C before further procedures.
Extracted molecule total RNA
Extraction protocol Total RNA samples were isolated from the cultured skin fibroblasts with the use of MagNa Pure Compact RNA Isolation Kit (Roche Applied Science, Mannheim, Germany). Quantity and quality of RNA samples were assessed using the NanoDrop instrument (Thermo Scientific) and evaluated with the RNA 6000 Nano Assay on the Agilent 2100 Bioanalyser (Agilent Technologies Inc., USA).
Label Biotin
Label protocol Ambion Illumina TotalPrep RNA Amplification Kit, according to manufacturer's instructions
 
Hybridization protocol Illumina® Whole-Genome Gene Expression Direct Hybridization Assay, according to manufacturer's instructions
Scan protocol HiScan SQ according to manufacturer's instructions
Description Fasting
Data processing The data was imported into Partek GS from Genoe Studio.
 
Submission date Dec 21, 2018
Last update date Apr 23, 2019
Contact name Agnieszka Lugowska
E-mail(s) alugipin@yahoo.com
Organization name Institute of Psychiatry and Neurology
Department Department of Genetics
Street address Al. Sobieskiego 9
City Warsaw
ZIP/Postal code 02-957
Country Poland
 
Platform ID GPL10904
Series (1)
GSE124283 Changes in the level of expression of genes involved in the pathogenic mechanisms in rare, inherited metabolic diseases.

Data table header descriptions
ID_REF
VALUE Log2 transformed, quantile normalized
3999844010_J.Detection Pval

Data table
ID_REF VALUE 3999844010_J.Detection Pval
7A5 81.82063 0.08181818
A1BG 81.83362 0.01773065
A1CF 79.41273 0.1497418
A26C3 76.6523 0.8906912
A2BP1 75.65798 0.9669521
A2LD1 116.3511 0
A2M 79.50161 0.2974026
A2ML1 76.93849 0.6675324
A3GALT2 76.46848 0.8016318
A4GALT 210.4553 0
A4GNT 78.48149 0.4246753
AAA1 77.40514 0.7051255
AAAS 92.51619 0.001298701
AACS 114.1886 0
AACSL 82.22108 0.06623377
AADAC 77.92901 0.5194805
AADACL1 181.3032 0
AADACL2 78.94119 0.3636364
AADACL3 79.44971 0.3064935
AADACL4 83.8951 0.03636364

Total number of rows: 31424

Table truncated, full table size 764 Kbytes.




Supplementary file Size Download File type/resource
GSM3526890_3999844010_J_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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