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Sample GSM2831696 Query DataSets for GSM2831696
Status Public on May 27, 2019
Title A5Ba/F3-gp130 cells (exon-level)
Sample type RNA
 
Source name A5Ba/F3-gp130 cells
Organism Mus musculus
Characteristics cell line: Ba/F3-gp130
cell line vendor: Ba/F3 (DSMZ no.: ACC 300)
cell type: Hyper-Interleukin-6 dependent pro-B cellline
transfection: untransfected
stimulation: unstimulated
Treatment protocol Ba/F3-gp130 cell lines were washed four times with sterile PBS and incubated in serum-free DMEM for 3 h. Equal numbers of cells (2 x 10^6) were stimulated for 1h at 37°C with 50µl GFP-PFC emulsion in 1ml serum free DMEM medium (1 h at 37°C). As a positive stimulation control Ba/F3-gp130 cells were incubated for 1h at 37°C with 100ng/ml Hyper IL-6 in serum free medium (Samples E2, E4, E6)
Growth protocol Ba/F3 cell lines were cultured in DMEM with 1% PenStrep and 10%FCS with recombinant Hyper-IL-6 (10 ng/ml cell culture supernatant) in 10 cm cell culture plattes and were splitted in a ratio from 1:10000 to 1:5
Extracted molecule total RNA
Extraction protocol Total RNA extraction was made with RNeasy mini kit (Qiagen, Hilden, Germany) including DNAse digestion according to the manufacturer's instructions. RNA quality was evaluated using an Agilent 2100 Bioanalyzer and only high quality RNA (RIN > 8) was used for microarray analysis.
Label biotin
Label protocol 150 ng total RNAwas amplified using the Ambion WT Expression Kit and the WT Terminal Labeling Kit (Affymetrix, Freiburg, Germany).
 
Hybridization protocol Amplified cDNA was hybridized on Affymetrix Mouse Gene ST 1.0 arrays (Affymetrix)
Scan protocol Detection of probe intensities was performed using a GeneChip scanner 3000 7G (GDAS 1.4 package, Affymetrix).
Description RNA expression value derived from Expression Console software; core-exon analysis
Data processing The data were analyzed with Affymetrix Expression Console using default analysis settings for RNA analyses for gene default and exon default .CHP files.
 
Submission date Oct 26, 2017
Last update date May 27, 2019
Contact name Birgit Knebel
Organization name German Diabetes Center
Department Cinical Biochemistry and Pathobiochemistry
Street address Auf'm Hennekamp 65
City Duesseldorf
ZIP/Postal code 40225
Country Germany
 
Platform ID GPL10740
Series (1)
GSE106215 Tracking of Individual Cell Populations by 19F MRI using a "Cargo Internalization Receptor (CIR)" System
Relations
Alternative to GSM2831664 (gene-level analysis)

Data table header descriptions
ID_REF
VALUE RMA signal
DETECTION P-VALUE

Data table
ID_REF VALUE DETECTION P-VALUE
10338001 12.1166 0
10338002 8.30041 0.185149
10338003 10.6409 0
10338004 9.27374 3.87328e-13
10338005 3.36631 0.859626
10338006 3.67395 0.57077
10338007 4.43348 0.877159
10338008 5.81594 0.962871
10338009 9.24217 0.350326
10338010 3.42889 0.597301
10338011 7.79522 0.48238
10338012 3.53775 0.0751862
10338013 3.21911 0.374594
10338014 3.27829 0.674761
10338015 3.24614 0.264681
10338016 9.25679 0.589328
10338017 13.4924 5.56014e-36
10338018 8.68239 0.618056
10338019 7.47281 0.45151
10338020 9.51204 0.910461

Total number of rows: 241576

Table truncated, full table size 6440 Kbytes.




Supplementary file Size Download File type/resource
GSM2831696_A5BaF3_gp130.CEL.gz 4.6 Mb (ftp)(http) CEL
GSM2831696_A5BaF3_gp130.exon_.rma-exon-default-dabg.chp.gz 2.2 Mb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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