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Sample GSM1290190 Query DataSets for GSM1290190
Status Public on May 19, 2014
Title BMDM(KO)_untreated_rep2
Sample type RNA
 
Source name BMDM(KO)_untreated
Organism Mus musculus
Characteristics individual: mouse#4
genotype: Commd1 knockout
treatment: untreated
cell type: Bone marrow derived macrophages
Treatment protocol Cells were treated with LPS (10ng/mL, Escherichia coli 026:B6, Sigma).
Growth protocol BMDMs were generated by isolation of bone marrow cells from long bones, which were cultured in RPMI supplemented with 10% FCS, antibiotics (penicillin G 100μg/mL and streptomycin 100μg/mL) and Fungizone (Fisher), in the presence of GM-CSF (20ng/ml, Peprotech). Myeloid differentiation was allowed to proceed for 10 days.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared by use of RNeasy Mini Kit (Qiagen).
Label Cy3
Label protocol Synthesis of Cy3-labeled cRNA was performed with the “Quick Amp Labeling kit, one color” (#5190-0442, Agilent Technologies) according to the manufacturer’s recommendations.
 
Hybridization protocol cRNA fragmentation, hybridization and washing steps were also carried-out exactly as recommended: “One-Color Microarray-Based Gene Expression Analysis Protocol V5.7”.
Scan protocol Slides were scanned on the Agilent Micro Array Scanner G2565CA (pixel resolution 5 µm, bit depth 20).
Data processing Data extraction was performed with the “Feature Extraction Software V10.7.3.1” by using the recommended default extraction protocol file: GE1_107_Sep09.xml. The single channel data generated by the Feature Extraction software were normalized and analyzed in Genespring GX software, version 12.0 (Agilent Technologies). Low expression values were raised to the constant value 15 (defined as threshold) to minimize false positive ratios. Data were log2 transformed, normalized to 75th percentile of each array according to the standard procedure in Genespring GX.
 
Submission date Dec 16, 2013
Last update date May 20, 2014
Contact name Oliver Dittrich-Breiholz
E-mail(s) dittrich.oliver@mh-hannover.de
Organization name Medical School Hannover
Department Research Core Unit Genomics
Street address Carl-Neuberg-Str. 1
City Hannover
ZIP/Postal code 30625
Country Germany
 
Platform ID GPL11202
Series (1)
GSE53368 Copper Metabolism Domain-Containing 1 Represses Genes That Promote Inflammation and Protects Mice From Colitis and Colitis-Associated Cancer

Data table header descriptions
ID_REF
VALUE Processed intensity values (log base 2)

Data table
ID_REF VALUE
A_51_P100034 3.5976248
A_51_P100174 -0.20263004
A_51_P100208 -7.256878
A_51_P100289 0.74671173
A_51_P100298 -1.5445137
A_51_P100309 -7.256878
A_51_P100327 -0.001844406
A_51_P100347 -7.256878
A_51_P100519 -7.256878
A_51_P100537 -7.0400352
A_51_P100573 0.27370453
A_51_P100624 -7.256878
A_51_P100625 -6.5200853
A_51_P100768 -7.256878
A_51_P100776 -6.7578993
A_51_P100787 2.63622
A_51_P100828 1.1557512
A_51_P100852 -0.46644402
A_51_P100991 -3.1135206
A_51_P100997 -4.3519597

Total number of rows: 39429

Table truncated, full table size 921 Kbytes.




Supplementary file Size Download File type/resource
GSM1290190_M4097.txt.gz 9.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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