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Sample GSM4192071 Query DataSets for GSM4192071
Status Public on Sep 15, 2020
Title Control mLSEC, biological rep5
Sample type RNA
 
Source name Control primary murine liver sinusoidal endothelial cells, biological replicate no 5
Organism Mus musculus
Characteristics cell type: Primary liver sinusoidal endothelial cells
treatment: Std 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 Std5
Gene expression data of control primary murine liver sinusoidal endothelial cells, 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 2.905273438
100009609_at 2.042480469
100009614_at 2.90625
100009664_at 2.540527344
100012_at 2.666503906
100017_at 7.14453125
100019_at 5.428710938
100033459_at 2.034667969
100034251_at 9.662109375
100034675_at 2.62109375
100034728_at 9.029296875
100034729_at 4.177734375
100034739_at 3.154785156
100034748_at 2.959960938
100036518_at 2.224609375
100036520_at 3.117675781
100036521_at 3.711425781
100036523_at 4.8359375
100036537_at 2.557128906
100036768_at 4.21484375

Total number of rows: 25428

Table truncated, full table size 530 Kbytes.




Supplementary file Size Download File type/resource
GSM4192071_Winkler_Derma_031218_Std5_MoGene-2_0-st_.CEL.gz 8.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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