NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1401300 Query DataSets for GSM1401300
Status Public on May 21, 2015
Title Wild type GM-DCs, replicate 3
Sample type RNA
 
Source name GM-DC derived from bone marrow and selected using CD11c microbeads
Organism Mus musculus
Characteristics strain: B6.129P2-Il2tm1Hor/J
cell type: GM-CSF myeloid dendritic cells
genotype: wild type
Treatment protocol Wt and IL-2-/- GM-DCs were treated or not with curdlan for 6h and processed for microarray
Growth protocol Bone marrow was flushed with IMDM medium with GM-CSF (200ng/ml), 1% Penicillin-Streptomycin, 10% Serum, 1% L-Glutamine and 0.1% β-Mercaptoethanol and cells were cultured for 7d The suspension cells were harvested on d7 and purified by positive selection using CD11c microbeads (Miltenyi Biotec) according to the manufacturer’s protocol. GM-DC (CD11c+, MHCII aI-A/I-E +) purity determined by FACS was routinely >95%.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted following the double extraction protocol using Trizol and Qiagen RNeasy Micro Extraction Kit. Total RNA integrity was assessed by Agilent Bioanalyzer.
Label biotin
Label protocol Single-stranded DNA were prepared according to the Ambion WT Expression Kit from 100ng of total RNA. 5.5ug of ssDNA were fragmented and labeled using the Affymetrix GeneChip WT Terminal Labeling Kit.
 
Hybridization protocol Fragmented samples were hybridized according to Affymetrix guidelines for 17hr in 45°C on GeneChip Mouse Gene 1.0 ST Array; The arrays were then washed and stained using the standard fluidics protocol (FS450_0007) for gene arrays on the GeneChip Fluidics Station 450.
Scan protocol The mouse gene chips were scanned using GeneChip Scanner 3000. The images were analyzed using Expression Console and standard array quality controls analyses were carried out according to the instructions provided by Affymetrix.
Data processing CEL files were processed in Bioconductor using the xps package. Expression data was summarized at the transcript level and normalized using RMA. Log2 transformation was applied to the expression data.
 
Submission date May 30, 2014
Last update date May 22, 2015
Contact name Bernett Lee
E-mail(s) bernett_lee@immunol.a-star.edu.sg
Organization name Singapore Immunology Network
Street address 8A Biomedical Grove #03-06 Immunos
City NA
ZIP/Postal code 138648
Country Singapore
 
Platform ID GPL6246
Series (1)
GSE58120 Dendritic cell-derived IL-2 promotes apoptosis of terminally mature cells via a novel autocrine signaling pathway

Data table header descriptions
ID_REF
VALUE log2 RMA normalized expression values

Data table
ID_REF VALUE
10338001 11.70329015
10338003 9.998389756
10338004 8.801362409
10338017 12.71927458
10338025 8.786500555
10338026 12.99990947
10338029 9.661878401
10338035 8.729240821
10338036 9.108770296
10338037 4.265821936
10338041 10.90070167
10338042 9.94402241
10338044 11.9022265
10338047 7.497059004
10338056 3.982667574
10338059 13.00594088
10338060 4.212586013
10338063 4.154681956
10338064 6.522916296
10338065 7.515571125

Total number of rows: 34760

Table truncated, full table size 709 Kbytes.




Supplementary file Size Download File type/resource
GSM1401300_M3160.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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