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Sample GSM371667 Query DataSets for GSM371667
Status Public on Aug 03, 2009
Title Monocyte_Ly6Chi_Blood_02
Sample type RNA
Source name Monocyte Ly-6Chi, Blood
Organism Mus musculus
Characteristics strain: C57BL/6
gender: female
age: 8-12 weeks
tissue: Blood
cell type: monocyte
monocyte subset: Ly6Chi
cell signature: Ly-6Chi monocytes were identified as CD11bhi (CD90/B220/CD49b/NK1.1/Ly-6G)lo (F4/80/I-Ab/CD11c)lo
Biomaterial provider C57BL/6 mice were purchased from The Jackson Laboratory, Bar Harbor, Maine 04609 USA
Treatment protocol healthy mice, no treatment
Growth protocol CHOW
Extracted molecule total RNA
Extraction protocol Monocyte subsets from blood and spleen of a group of four mice were isolated by fluorescence activated cell sorting (FACS) as CD11bhi (CD90/B220/CD49b/NK1.1/Ly-6G)lo (F4/80/I-Ab/CD11c)lo Ly-6Chi cells.
Samples of 1,000 Ly-6Chi blood and Ly-6Chi splenic monocytes were collected directly into 20 µl lysis buffer of the PicoPure RNA isolation kit (Arcturus). RNA extraction was subsequently performed according to the manufacturer’s instructions (Arcturus).
Total RNA quality was assessed using RNA pico lab chips on the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA). RIN (RNA integrity number) >= 8.
Label Cy3
Label protocol RNA was amplified using the NuGen WT-Ovation Pico System, and the amplified cDNA was labeled using the FL-Ovation cDNA Fluorescent Module (NuGen Technologies, San Carlos, Ca). 5ng of input total RNA was reverse–transcribed into cDNA and then amplified using a linear isothermal amplification process (SPIA). The amplified products were CY-3 labeled and fragmented according to manufacturer’s guidelines.
Hybridization protocol Labeled cDNA was assessed using the Nanodrop ND-100 (Nanodrop Technologies, Inc., Wilmington DE) and the Agilent 2100 Bioanalyzer; equal amounts of Cy3-labeled target were hybridized to Agilent whole mouse genome 4x44K Ink-jet arrays. Hybridizations were performed for 14 h according to the manufacturers protocol.
Scan protocol Arrays were scanned using the Agilent microarray scanner. Raw signal intensities were extracted with their Feature Extraction v9.1 software.
Description Sample preparation, labeling, and array hybridizations were performed according to standard protocols from the UCSF Shared Microarray Core Facilities and Agilent Technologies ( and
Data processing The dataset was normalized using the quantile normalization method. No background subtraction was performed, and the median feature pixel intensity was used as the raw signal before normalization. All procedures were carried out using functions in the R package limma in Bioconductor.
Submission date Feb 16, 2009
Last update date Sep 26, 2011
Contact name Martin Etzrodt
Phone (617) 643-0500
Fax (617) 643-6133
Organization name Massachusetts General Hospital
Department Center for Systems Biology
Lab Pittet Lab
Street address 185 Cambridge Street
City Boston
State/province MA
ZIP/Postal code 02114
Country USA
Platform ID GPL7202
Series (3)
GSE14850 Microarray analysis of splenic reservoir monocytes and their blood counterparts
GSE32364 Murine blood monocyte subsets
GSE32392 Regulation of Monocyte Functional Heterogeneity by miR-146a

Data table header descriptions
VALUE normalized signal

Data table
A_52_P616356 7.339850003
A_52_P580582 7.263247586
A_52_P403405 6.724940118
A_52_P819156 7.494855584
A_51_P331831 7.499128928
A_51_P430630 7.091665224
A_52_P502357 6.214926188
A_52_P299964 6.688687423
A_51_P356389 8.773004716
A_52_P684402 10.14477124
A_51_P414208 6.322491538
A_51_P280918 6.85190319
A_52_P613688 9.186272266
A_52_P258194 7.203348003
A_52_P229271 8.766508464
A_52_P214630 6.146568676
A_52_P579519 6.741045577
A_52_P979997 6.400345797
A_52_P453864 6.203509191
A_52_P655842 6.63481105

Total number of rows: 41174

Table truncated, full table size 991 Kbytes.

Supplementary file Size Download File type/resource
GSM371667.txt.gz 9.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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