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Sample GSM773369 Query DataSets for GSM773369
Status Public on Nov 16, 2012
Title Donor # 340 from monocytes deriving from apheresis # 1 manufacture 2 hybridized on slide # 5729 position 2
Sample type RNA
 
Channel 1
Source name mature Dendritic Cells of Donor
Organism Homo sapiens
Characteristics cell type: mature Dendritic Cells
donor: 340
apheresis: 1
manufacture: 2
slide #: 5729
position # on slide: 2
Growth protocol Monocytes were cultured with GMCSF (1000 IU/ml) and IL4 (1000 IU/ml) for 3 days to obtain immature dendritic cells. To induce maturation LPS (30 ng/ml) and IFNg (1000 IU/ml) were added to the culture and cell were harvested 24 h later
Extracted molecule total RNA
Extraction protocol Total RNA extracted using miRNeasy kit from Qiagen
Label Cy5
Label protocol Test RNA and Universal Reference RNA () were amplified and labeled according to the Two-color Microarray-based Gene Expression Analysis (quick Amp Labeling) protocol from Agilent Version 5.7
 
Channel 2
Source name Universal Human Reference RNA
Organism Homo sapiens
Characteristics sample type: reference
vendor: Stratagene Catalog #740000
Growth protocol Monocytes were cultured with GMCSF (1000 IU/ml) and IL4 (1000 IU/ml) for 3 days to obtain immature dendritic cells. To induce maturation LPS (30 ng/ml) and IFNg (1000 IU/ml) were added to the culture and cell were harvested 24 h later
Extracted molecule total RNA
Extraction protocol Total RNA extracted using miRNeasy kit from Qiagen
Label Cy3
Label protocol Test RNA and Universal Reference RNA () were amplified and labeled according to the Two-color Microarray-based Gene Expression Analysis (quick Amp Labeling) protocol from Agilent Version 5.7
 
 
Hybridization protocol Samples were hybridized according to the Two-color Microarray-based Gene Expression Analysis (quick Amp Labeling) protocol from Agilent Version 5.7
Scan protocol Scanned on an Agilent G2565BA scanner.
Images were quantified using Agilent Feature Extraction Software
Description mature Dendritic Cells of Donor # 340 from monocytes deriving from apheresis # 1 manufacture 2 hybridized on slide # 5729 position 2
Data processing Agilent Feature Extraction Software was used with dafault settings for processed signals
 
Submission date Aug 03, 2011
Last update date Nov 17, 2012
Contact name Luciano Castiello
E-mail(s) castiellol@cc.nih.gov
Phone 3014356380
Fax 3014358643
Organization name NIH/CC
Department DTM
Lab CPS
Street address 10 Center Drive
City Bethesda
State/province Maryland
ZIP/Postal code 20892
Country USA
 
Platform ID GPL4133
Series (1)
GSE31195 Study of the consistency, comparability and identity of different Dendritic cells productions for clinical use

Data table header descriptions
ID_REF
VALUE normalized log10 ratio Cy5/Cy3

Data table
ID_REF VALUE
1 3.947532571e-001
2 0.000000000e+000
3 0.000000000e+000
4 0.000000000e+000
5 0.000000000e+000
6 0.000000000e+000
7 0.000000000e+000
8 0.000000000e+000
9 0.000000000e+000
10 0.000000000e+000
11 0.000000000e+000
12 5.903872945e-001
13 5.708536078e-001
14 5.661972811e-002
15 -8.106789327e-002
16 2.644413818e-001
17 -9.388362826e-002
18 1.302733897e-001
19 -3.225646525e-001
20 -2.602488120e-002

Total number of rows: 45015

Table truncated, full table size 1019 Kbytes.




Supplementary file Size Download File type/resource
GSM773369.txt.gz 14.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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