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Sample GSM3526982 Query DataSets for GSM3526982
Status Public on Apr 23, 2019
Title Fasting 3999853050_F
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: 26/00
viability: alive
condition: NPC-N
gender: M
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
3999853050_F.Detection Pval

Data table
ID_REF VALUE 3999853050_F.Detection Pval
7A5 77.23869 0.4168831
A1BG 82.01122 0.007934728
A1CF 76.51091 0.5243393
A26C3 79.06835 0.2831434
A2BP1 75.8848 0.7076761
A2LD1 94.64553 0
A2M 80.2089 0.112987
A2ML1 73.31568 0.8818182
A3GALT2 75.09856 0.802449
A4GALT 180.685 0
A4GNT 77.62247 0.3623376
AAA1 74.2824 0.97163
AAAS 122.4326 0
AACS 115.3856 0
AACSL 85.5517 0.005194805
AADAC 78.73977 0.238961
AADACL1 174.6116 0
AADACL2 78.49197 0.2558441
AADACL3 79.82473 0.1324675
AADACL4 76.18901 0.5597402

Total number of rows: 31424

Table truncated, full table size 752 Kbytes.




Supplementary file Size Download File type/resource
GSM3526982_3999853050_F_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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