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Sample GSM3386201 Query DataSets for GSM3386201
Status Public on Nov 05, 2018
Title Control mLSEC biological rep2
Sample type RNA
 
Source name Control primary murine liver sinusoidal endothelial cells, biological replicate no 2
Organism Mus musculus
Characteristics genotype: Ctrl
tissue: liver
cell type: sinusoidal endothelial cells
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 Clec4g-Cre(tg/wt) mice were crossed with Rosa26-N1ICD-IRES-GFP mice to generate Clec4g-Cre(tg/wt);Rosa26-N1ICD-IRES-GFP mice (NICD-OE-HEC).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with innuPREP RNA Mini Kit (Analytik Jena).
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 control primary murine liver sinusoidal endothelial cells
Data processing The data were analyzed with a commercial software called JMP Genomics, version 7, 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 Sep 12, 2018
Last update date Nov 05, 2018
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 (1)
GSE119875 Expression data from Notch intracellular domain overexpressing primary murine liver sinusoidal endothelial cells

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
100009600_at 2.727539063
100009609_at 1.644042969
100009614_at 2.345703125
100009664_at 2.163574219
100012_at 2.052734375
100017_at 6.346679688
100019_at 4.576171875
100033459_at 2.248046875
100034251_at 8.1640625
100034675_at 2.290527344
100034728_at 8.36328125
100034729_at 4.163085938
100034739_at 2.350585938
100034748_at 2.393066406
100036518_at 1.338378906
100036520_at 3.517089844
100036521_at 3.371582031
100036523_at 5.091796875
100036537_at 2.235839844
100036768_at 4.33203125

Total number of rows: 25428

Table truncated, full table size 532 Kbytes.




Supplementary file Size Download File type/resource
GSM3386201_Winkler_Derma_100718_Ctrl_2_MoGene-2_0-st_.CEL.gz 7.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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