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Sample GSM11002 Query DataSets for GSM11002
Status Public on Oct 06, 2003
Title AcB55 #12262264
Sample type RNA
 
Channel 1
Source name Spleen of AcB55 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) [email protected]
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 0.1626061 7093.284 6028.7656
2 0.014105974 1769.9319 1745.1406
3
4
5
6 -0.25079557 256.76135 329.9505
7 -0.6447939 1103.2954 2102.4333
8 -0.07103106 854.125 917.001
9 -0.33820757 408.7159 573.1961
10 -0.05603299 183.875 194.47218
11 -0.20632489 510.0909 626.9795
12 -0.08601563 17904.762 19513.027
13 -0.12429034 9896.408 11206.145
14 0.18414295 3059.5908 2545.0193
15 0.34278592 1627.7273 1155.3448
16 -0.6940043 1569.5 3141.6917
17 -0.7490787 2716.6138 5745.7754
18 -0.7712484 438.125 947.4297
19 0.19235717 3431.4773 2831.0105
20 -0.59823817 4543.864 8264.885

Total number of rows: 15247

Table truncated, full table size 512 Kbytes.




Supplementary data files not provided

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