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Sample GSM4043951 Query DataSets for GSM4043951
Status Public on Aug 27, 2019
Title Hepa1-6, Oleic acid treatment
Sample type RNA
 
Source name Hepa1-6 cells
Organism Mus musculus
Characteristics treatment: Oleic acid (500 µM)
Treatment protocol Hepa1-6 cells were seeded and incubated overnight, followed by treatment with 500 µM concentration of fatty acids for 24 hrs. All fatty acid stocks were initially reconstituted in absolute ethanol. Sub-stocks of fatty acids at 25 mM were prepared in filter-sterilised KOH at 70 mM. Complete DMEM supplemented with fatty acid-free bovine serum albumin (BSA; Sigma-Aldrich, St. Louis, MO) were filter sterilised, and incubated for 30 min with fatty acids to complex BSA to fatty acids. Ratio of BSA to fatty acids were approximately 1:2. Vehicle control treatments only contained equivalent mixture of ethanol and KOH.
Growth protocol Hepa1-6 cells (# CRL-1830) were obtained from American Type Culture Collection (ATCC; Manassas, VA) and cultured in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin and 1000 µg/mL streptomycin (Lonza, Verviers, Belgium) in a humidified chamber at 37oC with 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from samples using the RNeasy kit (Qiagen) with a DNase digestion step according to the manufacturer’s protocol. RNA quality was verified on an Agilent 2100 Bioanalyzer (Agilent Technologies, Amsterdam, The Netherlands) using 6000 Nano Chips according to manufacturer’s instructions. RNA was considered suitable for array hybridization only if RNA integrity number exceeded 8.0. RNA from 6 samples per group was pooled for microarray analysis
Label biotin
Label protocol Total RNA (100ng per sample) was labeled with the Whole-Transcript Sense Target Assay (Affymetrix, Santa Clara, CA, USA; P/N 900652).
 
Hybridization protocol Hybridization and washing of the Affymetrix GeneChip Mouse Gene 2.1 ST peg arrays were performed on a GeneTitan Instrument according to the manufacturer's recommendations (Affymetrix, Santa Clara, CA, USA).
Scan protocol Arrays were scanned on an Affymetrix GeneTitan instrument (Affymetrix, Santa Clara, CA, USA).
Data processing Expression estimates were calculated applying the RMA algorithm in the Bioconductor library 'Oligo' (v1.46.0).
 
Submission date Aug 23, 2019
Last update date Aug 28, 2019
Contact name Guido Hooiveld
E-mail(s) [email protected]
Organization name Wageningen University
Department Div. Human Nutrition & Health
Lab Nutrition, Metabolism & Genomics Group
Street address HELIX, Stippeneng 4
City Wageningen
ZIP/Postal code NL-6708WE
Country Netherlands
 
Platform ID GPL17400
Series (2)
GSE136278 Industrial trans fatty acids stimulate SREBP2-mediated cholesterogenesis and promote non-alcoholic fatty liver disease [Hepa1-6 cells]
GSE136354 Industrial trans fatty acids stimulate SREBP2-mediated cholesterogenesis and promote non-alcoholic fatty liver disease

Data table header descriptions
ID_REF
VALUE RMA signal (as log2)

Data table
ID_REF VALUE
17200001 5.258492509
17200003 4.360365411
17200005 4.507369625
17200007 3.144250231
17200009 5.384173092
17200011 3.392126598
17200013 3.374231344
17200015 4.824634537
17200017 1.421373372
17200019 2.05823286
17200021 2.875943924
17200023 4.554962538
17200025 3.457699126
17200027 4.652187913
17200029 3.856299053
17200031 2.920396456
17200033 1.942540075
17200035 2.199722822
17200037 3.071283213
17200039 1.865580647

Total number of rows: 41345

Table truncated, full table size 843 Kbytes.




Supplementary file Size Download File type/resource
GSM4043951_G260_G07_Oleic.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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