NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM99341 Query DataSets for GSM99341
Status Public on Sep 22, 2006
Title B-CLL sample 813, 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 784.5 P 0.000662
AFFX-BioB-M_at 1578.2 P 0.000052
AFFX-BioB-3_at 684.9 P 0.000857
AFFX-BioC-5_at 2571.7 P 0.00007
AFFX-BioC-3_at 2321.1 P 0.000052
AFFX-BioDn-5_at 1941.4 P 0.000044
AFFX-BioDn-3_at 12363.2 P 0.00007
AFFX-CreX-5_at 26398.2 P 0.000044
AFFX-CreX-3_at 37200.6 P 0.000044
AFFX-DapX-5_at 91.8 A 0.139482
AFFX-DapX-M_at 40.2 A 0.559354
AFFX-DapX-3_at 7.1 A 0.937071
AFFX-LysX-5_at 1.4 A 0.937071
AFFX-LysX-M_at 10.7 A 0.814869
AFFX-LysX-3_at 21.7 A 0.544587
AFFX-PheX-5_at 10.1 A 0.937071
AFFX-PheX-M_at 13.3 A 0.814869
AFFX-PheX-3_at 113.6 A 0.425962
AFFX-ThrX-5_at 17.1 A 0.712257
AFFX-ThrX-M_at 50.1 A 0.300606

Total number of rows: 22283

Table truncated, full table size 598 Kbytes.




Supplementary data files not provided

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