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Sample GSM3526999 Query DataSets for GSM3526999
Status Public on Apr 23, 2019
Title Fasting 3999853053_K
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: K18
viability: alive
condition: Control
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
3999853053_K.Detection Pval

Data table
ID_REF VALUE 3999853053_K.Detection Pval
7A5 78.18716 0.4155844
A1BG 79.17603 0.2167726
A1CF 76.23534 0.8300656
A26C3 76.95237 0.667448
A2BP1 77.94751 0.3918776
A2LD1 128.9109 0
A2M 84.89906 0.01428571
A2ML1 75.73808 0.7350649
A3GALT2 76.58469 0.7250456
A4GALT 122.4417 0
A4GNT 82.76109 0.05324675
AAA1 78.85876 0.221077
AAAS 93.4409 0
AACS 105.5115 0
AACSL 84.98846 0.01298701
AADAC 75.14241 0.8077922
AADACL1 112.1695 0
AADACL2 78.12224 0.4220779
AADACL3 77.9856 0.438961
AADACL4 83.07301 0.04805195

Total number of rows: 31424

Table truncated, full table size 754 Kbytes.




Supplementary file Size Download File type/resource
GSM3526999_3999853053_K_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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