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Sample GSM11008 Query DataSets for GSM11008
Status Public on Oct 06, 2003
Title AcB61 #12250554
Sample type RNA
 
Channel 1
Source name Spleen of AcB61 mice
Organism Mus musculus
Extracted molecule total RNA
 
Channel 2
Source name Spleen of A/J mice
Organism Mus musculus
Extracted molecule total RNA
 
 
Description Animals were sacrificed and organs were rapidly frozen in liquid nitrogen, and subsequently stored at <ETH>80oC. Tissues were mechanically homogenized with a polytron and total cellular RNA was extracted using a commercially available reagent (TMTRIzol; Invitrogen). The poly-(A)+ fraction of the RNA was isolated by chromatography with oligo d(T) cellulose beads. For cDNA labeling, either 25 mg of total RNA or 2.5 mg of poly-(A) RNA was converted into cDNA using reverse transcriptase (RT; Super Script II, Invitrogen) and alternatively Cy5 or Cy3-labeled dCTP (1mM, Perkin Elmer-Cetus/NEN, Boston) in a reaction mixture containing 1.5 mL oligo (dT) (100pmol/ mL), 3 mL dNTP-dCTP (6.67mM each), 1 mL dCTP (2mM), 4 mL DTT (100mM), 8 mL 5 X RT Buffer (Invitrogen, California). The reactions were carried out at 42¼C for 3 hrs, after which the RNA was degraded by the addition of 0.5 mL RNase A (1 mg/mL) and 1.5 mL RNaseH 5 units/mL). Labeled cDNA was separated from unincorporated nucleotides (Qiagen column) and further concentrated by evaporation under vacuum.
The arrays were pre-hybridized for 1-2hrs with DIGEasy hybridization buffer (Roche) containing 10ug/ml denatured salmon sperm DNA, and 10ug/ml yeast tRNA. The Cy5 and Cy3 labelled cDNAs were combined and hybridized in the same medium and incubated with the arrays for 16-18hrs at 37Co. Finally, the arrays were washed 3 x 10 mins in 0.1 x SSC (20 X SSC is 3M sodium chloride, 0.3 M sodium citrate, pH 7.0), 0.1%SDS at 50Co, and 4 x 3min in 0.1 x SSC at room temperature, and dried by centrifugation.
Fluorescent array images were collected for both Cy3 and Cy5 with a ScanArray fluorescent scanner and image intensity data were extracted and analyzed with QuantArray 3.0 analysis software. Quantification data was imported in GeneSpring (Silicon Genetics). The import format was modified to maintain information relevant to user-contributed flagging as well as QC parameter furnished by the array manufacturer. Dye swap and Intensity-based normalization (Lowess) were performed using the default settings.
Keywords = spleen
Keywords = malaria
 
Submission date Oct 04, 2003
Last update date Oct 28, 2005
Contact name Gundula Min-Oo
E-mail(s) gundula.min-oo@mail.mcgill.ca
Phone 5143982542
Organization name McGill University
Department Biochemistry
Street address
City Montreal
State/province Quebec
ZIP/Postal code H3G 1Y6
Country Canada
 
Platform ID GPL519
Series (1)
GSE709 Malaria resistance

Data table header descriptions
ID_REF
VALUE Normalized log ratio of means defined by CH1/ CH2
CH1_MEAN mean normalized fluorescence intensity of experimental sample
CH2_MEAN mean normalized fluorescence intensity of control sample

Data table
ID_REF VALUE CH1_MEAN CH2_MEAN
1 0.012170459 11486.932 11347.978
2 0.21701528 742.2727 597.46844
3
4
5
6 0.027201325 364.82953 355.03946
7 -0.1292972 422.85226 481.2178
8 0.04913883 333.26135 317.28113
9 -0.1388971 483.82953 555.923
10 -0.068543315 564.7727 604.8417
11 -0.17880143 288.8409 345.3911
12 -0.02063814 1377.8069 1406.5377
13 0.54015976 571.6477 333.0735
14 0.19526859 371.10226 305.2738
15 0.54139185 834.03406 485.3559
16 0.09057365 1411.8181 1289.5647
17 0.09063223 2129.8066 1945.2664
18 -0.075114034 468.13635 504.6543
19 -0.12676865 1648.0342 1870.7732
20 -0.51800025 1811.1135 3040.257

Total number of rows: 15247

Table truncated, full table size 514 Kbytes.




Supplementary data files not provided

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