GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM658010 Query DataSets for GSM658010
Status Public on Mar 01, 2011
Title Control PB C106
Sample type RNA
Source name Control PB C106
Organism Homo sapiens
Characteristics disease state: Control
tissue: peripheral blood
Growth protocol Peripheral blood from B-CLL patients as well as from healthy donors were firstly separated by Ficoll gradient (GE Healthcare), obtained peripheral mononuclear cells (PBMC). PBMC were shortly incubated in IMDM (Isove’s Modified Dulbecco’s) medium supplemented with 10% fetal calf serum, 1% non essential amino acids, 1% antibiotics. PBMCs from healthy donors were separated by autoMACS Pro Separator and anti FITC microbeads, CD19 human FITC antibody were used.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted by TRIzol Reagent following the manufacturer protocol. Precipitation by isopropyl alcohol (0.5mL per 1mL TRIzol) was done over night. As carrier of the aqueous phase the Acrylamide was used. The RNA pellets were washed with 75% ethanol (1mL per 1mL TRIzol) and dry pellets were resuspend in 20 uL of RNAse free water.
Label biotin
Label protocol RNA was proceeded according to Affymetrix 3‘ – IVT Express Kit protocol. cDNA were prepared using the recommended Affymetrix reagents and kits.
Hybridization protocol RNA was proceeded according to Affymetrix 3‘ – IVT Express Kit protocol. cDNA was hybridized for 16 hr to the Affymetrix array as described in the Expression Analysis Technical Manual. GeneChips were washed and stained in the Affymetrix Fluidics Station.
Scan protocol GeneChips were processed using the Agilent GeneArray Scanner 3000 7G system in the Genomics Facility of the New York University Cancer Institute.
Data processing Data were summarized using GeneSpring implementation of RMA algorithm and expression data were normalized on median of control samples.
Submission date Jan 19, 2011
Last update date Sep 01, 2016
Contact name Vojtěch Kulvait
Phone +420224965968
Organization name Charles University in Prague - 1st Faculty of Medicine
Department Institute of Pathological Physiology
Lab Centrum for experimental haematology
Street address U Nemocnice 5
City Prague 2
ZIP/Postal code 128 53
Country Czech Republic
Platform ID GPL570
Series (1)
GSE26725 Gene expression analysis of 12 B-cell Chronic Lymphocytic Leukemia samples and 5 CD19+ control samples
Reanalyzed by GSE86362

Data table header descriptions
VALUE RMA algorithm and expression data were normalized on median of control samples

Data table
AFFX-BioB-5_at 0.42370987
AFFX-BioB-M_at 0.35147858
AFFX-BioB-3_at 0.37071133
AFFX-BioC-5_at 0.3070259
AFFX-BioC-3_at 0.33587742
AFFX-BioDn-5_at 0.17649555
AFFX-BioDn-3_at 0.19546795
AFFX-CreX-5_at 0.06708336
AFFX-CreX-3_at 0.074279785
AFFX-DapX-5_at 0.11415434
AFFX-DapX-M_at 0.26837826
AFFX-DapX-3_at 0.059249878
AFFX-LysX-5_at -0.09236455
AFFX-LysX-M_at -0.016587734
AFFX-LysX-3_at 0.11053753
AFFX-PheX-5_at 0.37480855
AFFX-PheX-M_at 0.13104463
AFFX-PheX-3_at -0.0077364445
AFFX-ThrX-5_at 0.0
AFFX-ThrX-M_at 0.23012161

Total number of rows: 54675

Table truncated, full table size 1115 Kbytes.

Supplementary file Size Download File type/resource
GSM658010_C106.CEL.gz 4.3 Mb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table

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