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Sample GSM3527022 Query DataSets for GSM3527022
Status Public on Apr 23, 2019
Title Fasting 3999853055_J
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: K21
viability: alive
condition: Control
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
3999853055_J.Detection Pval

Data table
ID_REF VALUE 3999853055_J.Detection Pval
7A5 78.07611 0.6610389
A1BG 80.5531 0.2333243
A1CF 78.56777 0.6800569
A26C3 79.24349 0.5048701
A2BP1 78.76308 0.6464123
A2LD1 140.7032 0
A2M 109.309 0
A2ML1 81.53539 0.2181818
A3GALT2 81.37913 0.3304739
A4GALT 156.0316 0
A4GNT 84.0836 0.05584415
AAA1 79.07484 0.4416167
AAAS 103.1916 0
AACS 111.4724 0
AACSL 84.68804 0.04025974
AADAC 79.72009 0.448052
AADACL1 138.9332 0
AADACL2 78.72516 0.5636364
AADACL3 77.58411 0.7298701
AADACL4 77.82275 0.6961039

Total number of rows: 31424

Table truncated, full table size 757 Kbytes.




Supplementary file Size Download File type/resource
GSM3527022_3999853055_J_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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