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Sample GSM3527007 Query DataSets for GSM3527007
Status Public on Apr 23, 2019
Title Stand. 3999853054_G
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: ME
viability: nie alive
condition: Gaucher
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 Stand.
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
3999853054_G.Detection Pval

Data table
ID_REF VALUE 3999853054_G.Detection Pval
7A5 77.87585 0.4896104
A1BG 85.32943 0.02026058
A1CF 78.29251 0.4033276
A26C3 78.42223 0.3721723
A2BP1 77.56104 0.5749344
A2LD1 111.9937 0
A2M 77.09916 0.6038961
A2ML1 77.24261 0.5831169
A3GALT2 80.02428 0.2219337
A4GALT 149.8404 0
A4GNT 82.45277 0.06363636
AAA1 79.94774 0.05805364
AAAS 123.4775 0
AACS 101.9021 0
AACSL 84.69689 0.01298701
AADAC 77.77345 0.5051948
AADACL1 391.376 0
AADACL2 77.09634 0.6064935
AADACL3 74.81188 0.8753247
AADACL4 80.00589 0.2441558

Total number of rows: 31424

Table truncated, full table size 753 Kbytes.




Supplementary file Size Download File type/resource
GSM3527007_3999853054_G_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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