NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4192066 Query DataSets for GSM4192066
Status Public on Sep 15, 2020
Title CDAA mLSEC, biological rep5
Sample type RNA
 
Source name Primary murine liver sinusoidal endothelial cells after 10 weeks of CDAA diet, biological replicate no 5
Organism Mus musculus
Characteristics cell type: Primary liver sinusoidal endothelial cells
treatment: CDAA diet
treatment duration: 10 days
Treatment protocol Livers were perfused in situ through the portal vein with a collagenase/amino acid/saccharide solution (Sigma-Aldrich), dissected, mechanically disrupted, pooled from 3 mice, digested for 25 minutes at 38 °C in collagenase/Gey’s balanced salt solution (Sigma-Aldrich), and filtered through a mesh. Nonparynchymal cells were separated by a 19.3% Nycodenz gradient. Afterward, liver sinusoidal endothelial cells (LSEC) were isolated by Magnetic-activated cell sorting (MACS) using CD146 MicroBeads (Miltenyi) according to manufacturers’ instructions.
Growth protocol Ten-week-old female C57BL/6N mice and control siblings were fed a CDAA diet containing 31% of fat per calorie and 1% cholesterol (E15666-94, Ssniff) or a control diet (V1534-000, Ssniff) for ten weeks.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with innuPREP RNA Mini Kit (Analytik Jena), then treated with TURBO DNA-free Kit (Invitrogen).
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 CDAA5
Gene expression data of primary murine liver sinusoidal endothelial cells after 10 weeks of CDAA diet, biological replicate no 5
Data processing The data were analyzed with a commercial software called JMP Genomics, version 8, from SAS. Gene expression profiling was performed using arrays of mouse Mogene-2_0-type from Affymetrix. A Custom CDF Version 22 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 Nov 25, 2019
Last update date Sep 16, 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 GPL24557
Series (2)
GSE140994 Expression data of primary murine liver sinusoidal endothelial cells after 10 weeks of CDAA diet
GSE141004 Expression data of murine liver sinusoidal endothelial cells

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
100009600_at 2.914550781
100009609_at 2.456054688
100009614_at 3.005859375
100009664_at 2.16015625
100012_at 2.410644531
100017_at 7.390625
100019_at 4.779296875
100033459_at 2.466308594
100034251_at 9.326171875
100034675_at 2.484375
100034728_at 9.892578125
100034729_at 1.724121094
100034739_at 2.651855469
100034748_at 3.064453125
100036518_at 1.985351563
100036520_at 3.633789063
100036521_at 3.802246094
100036523_at 5.462890625
100036537_at 2.965332031
100036768_at 4.463867188

Total number of rows: 25428

Table truncated, full table size 530 Kbytes.




Supplementary file Size Download File type/resource
GSM4192066_Winkler_Derma_031218_CDAA5_MoGene-2_0-st_.CEL.gz 8.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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