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Sample GSM99344 Query DataSets for GSM99344
Status Public on Sep 22, 2006
Title B-CLL sample 621, good prognosis
Sample type RNA
 
Source name immunomagnetically purified fresh CD19+ peripheral blood CLL cells
Organism Homo sapiens
Characteristics immunomagnetically purified native B-CLL cells from the peripheral blood of untreated patients

Treatment protocol no treatment
Growth protocol no in vitro culture
Extracted molecule total RNA
Extraction protocol Isolation of total RNA was performed with QIAGEN Rneasy columns according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at 45C on HG-U133A Arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Aim: to compare the transcriptosomes of good prognosis CLL cases (ZAP-70-CD38-) to poor prognosis cases (ZAP-70+CD38+). Methods: Immunomagnetic isolation was done using MidiMacs resulting in >95% purity of leukemic cells as detected by FACS analysis of CD19+CD5+ cells. The leukemic cells were freshly purified from untreated patients and RNA was directly isolated from fresh cells without further ex vivo treatment of the cells.Eight immunomagnetically purified peripheral blood derived ZAP-70+CD38+ CLL cases were compared with eight ZAP-70-CD38- B-CLL cases.
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1000.
 
Submission date Mar 07, 2006
Last update date Sep 22, 2006
Contact name Ludger Klein-Hitpass
E-mail(s) [email protected]
Phone +49 201 723 85552
Organization name Institut fuer Zellbiologie
Department Universitaetsklinikum
Lab BioChip Lab
Street address Virchowstr. 173
City Essen
ZIP/Postal code D-45122
Country Germany
 
Platform ID GPL96
Series (1)
GSE4392 Expression data from native ZAP-70+CD38+ vs. ZAP-70-CD38- CLL cells

Data table header descriptions
ID_REF
VALUE MAS5-calculated Signal intensity
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)
DETECTION P-VALUE 'detection p-value', p-value that indicates the significance level of the detection call

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 714.3 P 0.003212
AFFX-BioB-M_at 1364.3 P 0.000225
AFFX-BioB-3_at 523.8 P 0.003212
AFFX-BioC-5_at 2318.5 P 0.00011
AFFX-BioC-3_at 2080 P 0.000081
AFFX-BioDn-5_at 1751.7 P 0.000147
AFFX-BioDn-3_at 11040.9 P 0.000081
AFFX-CreX-5_at 21741.1 P 0.000044
AFFX-CreX-3_at 33848.9 P 0.000044
AFFX-DapX-5_at 16.2 A 0.724854
AFFX-DapX-M_at 125.8 A 0.239063
AFFX-DapX-3_at 21.3 A 0.860518
AFFX-LysX-5_at 34.5 A 0.340661
AFFX-LysX-M_at 10.9 A 0.814869
AFFX-LysX-3_at 54.4 A 0.672921
AFFX-PheX-5_at 9.9 A 0.949771
AFFX-PheX-M_at 9.4 A 0.949771
AFFX-PheX-3_at 132.9 A 0.39692
AFFX-ThrX-5_at 17.1 A 0.814869
AFFX-ThrX-M_at 87.6 A 0.440646

Total number of rows: 22283

Table truncated, full table size 599 Kbytes.




Supplementary data files not provided

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