NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4075758 Query DataSets for GSM4075758
Status Public on Apr 10, 2020
Title siCAV1+TGF-β rep 3
Sample type RNA
 
Source name primary hepatocytes treated with Cav1 siRNA and TGFBeta
Organism Mus musculus
Characteristics sirna: Caveolin-1
treatment: TGFBeta
Treatment protocol After attachment, primary hepatocytes were transfected overnight with 10 nM siRNA targeting CAV1 or a negative control siRNA using RNAiMAX transfection reagent according to the manufacturer’s instructions. Next day, the hepatocytes were treated with/without 5 ng/ml recombinant TGF-β1 and cultured additional 48 h in starvation medium.
Growth protocol Primary hepatocytes were prepared from 12 week old C57BL/6 mice via the two-step collagenase perfusion method.Then, isolated hepatocytes were plated on 6-well plates and cultured in Williams E medium with 1% l-glutamine, 1% Penicillin/Streptomycin, 0.1% dexamethasone and 10% fetal bovine serum. After hepatocyte attachment (~4 h), culture medium was changed to starvation medium (no dexamethasone and fetal bovine serum).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using InviTrap Spin Universal RNA Mini Kit from all sample groups according to the manufacturer’s instruction.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
 
Hybridization protocol Hybridization (16h x 45°C) was processed according to the standard Affymetrix protocol.
Scan protocol Affymetrix GeneArray Scanner3000
Description Gene expression data from mouse primary hepatocytes treated with Cav1 siRNA and TGFBeta
Data processing The data were analyzed with a commercial software called JMP Genomics, version 6, from SAS. Gene expression profiling was performed using arrays of mouse Mogene-1_0-type from Affymetrix. A Custom CDF Version 16 with Entrez based gene definitions was used to annotate the arrays. The Raw fluorescence intensity values were normalized applying quantile normalization, RMA background correction and Medianpolish Probeset Summary
 
Submission date Sep 12, 2019
Last update date Apr 10, 2020
Contact name Carsten Sticht
Organization name University Heidelberg
Department ZMF
Street address Theodor-Kutzer-Ufer
City Mannheim
ZIP/Postal code 68169
Country Germany
 
Platform ID GPL19485
Series (1)
GSE137339 Gene expression profiling of primary hepatocytes stimulated with TGF-β in the presence/absence of Caveolin-1

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
100008567_at 7.208007813
100009600_at 7.055664063
100009609_at 6.924804688
100009614_at 7.166015625
100012_at 6.963867188
100017_at 9.29296875
100019_at 7.755859375
100033459_at 6.9609375
100034251_at 6.99609375
100034748_at 7.133789063
100036520_at 7.139648438
100036521_at 7.518554688
100036523_at 7.426757813
100036537_at 7.208007813
100036768_at 7.0625
100037258_at 10.890625
100037260_at 7.202148438
100037262_at 7.317382813
100037278_at 7.571289063
100037396_at 7.147460938

Total number of rows: 21187

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM4075758_Meyer_270213_18-sicav_+48h_TGFbeta-IV_MoGene-1_0-st-v1_.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap