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Sample GSM11004 Query DataSets for GSM11004
Status Public on Oct 06, 2003
Title AcB61 #12243313
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 -0.21285258 8434.659 10435.379
2 0.33611682 802.6818 573.548
3
4
5
6 -0.067939885 328.90912 352.03177
7 -0.06380128 387.1591 412.66534
8 0.1708705 278.63635 234.87114
9 0.19358775 426.47726 351.41623
10 -0.022538083 761.1932 778.5438
11 0.028256694 250.38635 243.4103
12 -0.013514895 1459.0114 1478.8635
13 0.3999008 924.53406 619.7952
14 0.021328257 404.19318 395.66373
15 0.13826177 1113.9431 970.10046
16 0.14912862 1386.6023 1194.5001
17 0.20308605 3250.7046 2653.2512
18 -0.04935828 395.10226 415.09314
19 -0.13562785 1950.5114 2233.834
20 -0.42932242 1964.0568 3017.216

Total number of rows: 15247

Table truncated, full table size 516 Kbytes.




Supplementary data files not provided

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