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Sample GSM860541 Query DataSets for GSM860541
Status Public on Sep 05, 2012
Title Granulocytic monocytic progenitors_ healthy control_C0110N
Sample type RNA
 
Source name Healthy control_granulocytic monocytic progenitors (GMP)
Organism Homo sapiens
Characteristics age: 48
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 C0110N(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 GSM860609

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
7892501 5.593572
7892502 4.166451
7892503 3.272603
7892504 8.934742
7892505 2.984084
7892506 2.992319
7892507 2.517198
7892508 2.469229
7892509 10.90265
7892510 2.479665
7892511 2.986751
7892512 5.887558
7892513 3.025645
7892514 11.00376
7892515 9.686813
7892516 2.284159
7892517 3.643026
7892518 2.779907
7892519 5.647508
7892520 8.980739

Total number of rows: 33297

Table truncated, full table size 549 Kbytes.




Supplementary file Size Download File type/resource
GSM860541_US1-HuGene-1_0-ST-7573.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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