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Sample GSM860538 Query DataSets for GSM860538
Status Public on Sep 05, 2012
Title Granulocytic monocytic progenitors_ healthy control_C0109N
Sample type RNA
 
Source name Healthy control_granulocytic monocytic progenitors (GMP)
Organism Homo sapiens
Characteristics age: 52
tissue: bone marrow
karyotype: healthy control
Treatment protocol primary cells
Growth protocol primary cells
Extracted molecule total RNA
Extraction protocol Human bone marrow mononuclear cells were enriched for CD34 expression using Miltenyi MACS technology. Afterwards, cells were stained with antibodies against lineage-antigens (CD2, CD3,CD4, CD7, CD8, CD10, CD11b, CD14, CD19, CD20 CD56, Glycophorin A), CD34, CD38, CD90, as well as CD123 and CD45R in order to distinguish LT-HSC (Lin-/CD34+/CD38-/CD90+), ST-HSC (Lin-/CD34+/CD38-/CD90-), CMP (Lin-/CD34+/CD38+/CD123+/CD45R-), GMP (Lin-/CD34+/CD38+/CD123+/CD45R+) and MEP (Lin-/CD34+/CD38+/CD123-/CD45R-). Cells were subjected to 7-color 5 way sorting utilizing a high-speed cell sorter as previously described (Steidl et al., Nat Genet 2006). Total RNAwas extracted using a denaturing buffer containing guanidine isothiocyanate (ALLprep Kit, Qiagen) from sorted cell populations.
Label biotin
Label protocol 10 ng of total RNA were used for linear amplification of cDNA using the Ovation Pico RNA Amplification System (Nugen), according to the manufacturer's instructions. 5 µg of cRNA were biotin-labeled using the FL-Ovation cDNA Biotin Module V2 (NuGen).
 
Hybridization protocol Following fragmentation, labeled cRNA of each individual sample was hybridized to Affymetrix Affymetrix Human Gene 1.0 ST microarrays (Affymetrix) and stained according to the manufacturer's instructions.
Scan protocol Arrays were scanned according to the manufacturer's instructions.
Description C0109N(GMP)
Data processing Data were normalized normalized with the Expression Console Software version 1.1 from Affymetrix using Robust Multi-array Average (RMA) algorithm. MEV software was used to select differentially expressed genes by applying the following criteria: (a) Absolute value of the group mean difference greater than 1.5, and (b) p value smaller than 0.05 (Welch's t test)
 
Submission date Jan 11, 2012
Last update date Sep 05, 2012
Contact name Boris Bartholdy
Organization name Albert Einstein College of Medicine
Department Cell Biology
Street address 1300 Morris Park Ave
City Bronx
State/province NY
ZIP/Postal code 10461
Country USA
 
Platform ID GPL6244
Series (1)
GSE35008 Expression data from human hematopoietic stem and progenitor compartments from patients with acute myeloid leukemia with normal karyotype and healthy controls
Relations
Reanalyzed by GSM860606

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
7892501 6.798961
7892502 3.504065
7892503 3.295056
7892504 8.784557
7892505 3.139632
7892506 2.881966
7892507 4.909104
7892508 2.514012
7892509 10.83362
7892510 2.792446
7892511 3.482959
7892512 5.900045
7892513 3.010594
7892514 10.74284
7892515 10.35597
7892516 6.943286
7892517 4.794374
7892518 2.482544
7892519 5.212515
7892520 8.865047

Total number of rows: 33297

Table truncated, full table size 549 Kbytes.




Supplementary file Size Download File type/resource
GSM860538_US1-HuGene-1_0-ST-7570.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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