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Sample GSM3526895 Query DataSets for GSM3526895
Status Public on Apr 23, 2019
Title LDL+LPDS 3999844012_C
Sample type RNA
 
Source name skin fibroblasts
Organism Homo sapiens
Characteristics patient: DA
viability: deceased
condition: NPC-D
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 LDL+LPDS
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
3999844012_C.Detection Pval

Data table
ID_REF VALUE 3999844012_C.Detection Pval
7A5 77.64975 0.2688312
A1BG 79.99084 0.008773823
A1CF 75.47826 0.6033263
A26C3 75.66194 0.5418251
A2BP1 74.40905 0.8393995
A2LD1 107.8862 0
A2M 90.59802 0
A2ML1 72.39314 0.9233766
A3GALT2 78.43501 0.08261848
A4GALT 167.7124 0
A4GNT 76.9031 0.3662338
AAA1 74.61268 0.742757
AAAS 80.22861 0.05844156
AACS 93.89893 0
AACSL 76.05277 0.4597403
AADAC 75.87535 0.487013
AADACL1 133.7625 0
AADACL2 80.56759 0.04675325
AADACL3 75.31179 0.5675325
AADACL4 90.48389 0

Total number of rows: 31424

Table truncated, full table size 760 Kbytes.




Supplementary file Size Download File type/resource
GSM3526895_3999844012_C_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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