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Sample GSM658020 Query DataSets for GSM658020
Status Public on Mar 01, 2011
Title B-CLL PB P271
Sample type RNA
 
Source name B-CLL PB P271
Organism Homo sapiens
Characteristics disease state: B-CLL
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.
Description Additional information and characteristics in the referred paper supplement xls table.
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 Mar 01, 2011
Contact name Vojtěch Kulvait
E-mail(s) vojtech.kulvait@lf1.cuni.cz
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

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

Data table
ID_REF VALUE
AFFX-BioB-5_at -0.12312126
AFFX-BioB-M_at -0.113910675
AFFX-BioB-3_at -0.20144176
AFFX-BioC-5_at -0.17348099
AFFX-BioC-3_at -0.1398201
AFFX-BioDn-5_at -0.081445694
AFFX-BioDn-3_at -0.0746212
AFFX-CreX-5_at -0.03474903
AFFX-CreX-3_at -0.07304096
AFFX-DapX-5_at -0.13824725
AFFX-DapX-M_at -0.018806934
AFFX-DapX-3_at 0.008570433
AFFX-LysX-5_at 0.011413097
AFFX-LysX-M_at 0.14785504
AFFX-LysX-3_at 0.13085485
AFFX-PheX-5_at -0.07099247
AFFX-PheX-M_at -0.016021013
AFFX-PheX-3_at -0.012085915
AFFX-ThrX-5_at 0.10896659
AFFX-ThrX-M_at 0.08345127

Total number of rows: 54675

Table truncated, full table size 1175 Kbytes.




Supplementary file Size Download File type/resource
GSM658020_P271.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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