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Sample GSM11007 Query DataSets for GSM11007
Status Public on Oct 06, 2003
Title AcB61 #12249620
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 -0.44610545 10390.955 16232.918
2 -0.16977316 1666.25 1974.5663
3
4
5
6 -0.19528608 1075.1592 1307.0266
7 -0.030212985 1261.1477 1299.8322
8 -0.25963342 990.0796 1283.5934
9 0.16731949 1585.8864 1341.5477
10 -0.22007497 1611.8181 2008.5996
11 0.16195978 1304.7273 1109.6384
12 0.026874123 1962.3182 1910.2849
13 -0.0178876 1051.216 1070.1888
14 -0.119776554 1154.2727 1301.1481
15 -0.14750832 1226.2842 1421.1934
16 -0.28527346 1477.2158 1964.8826
17 -0.22651434 1810.7614 2271.0942
18 -0.22725217 1119.9204 1405.664
19 -0.4490765 2371.0342 3715.089
20 -0.3705956 1258.3523 1822.8456

Total number of rows: 15247

Table truncated, full table size 511 Kbytes.




Supplementary data files not provided

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