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Sample GSM10998 Query DataSets for GSM10998
Status Public on Oct 06, 2003
Title AcB55 #12256487
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) 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 -0.20810391 3786.4434 4662.4033
2 -0.16790763 601.4432 711.40344
3
4
5
6 -0.25519773 249.10228 321.5205
7 -0.18808028 3013.807 3637.455
8 -0.3823776 363.25 532.43933
9 -0.1431507 333.57953 384.91864
10 -0.090613164 202.46591 221.66887
11 -0.30659708 395.36365 537.2175
12 0.14329205 5434.8184 4709.2754
13 0.051767617 1641.6135 1558.7933
14 0.17741016 2130.7388 1784.3579
15 0.035496023 948.86365 915.77356
16 -0.24202514 1274.9431 1624.0559
17 -0.24567677 2054.6362 2626.8242
18 -0.25961757 411.51135 533.4974
19 0.024484504 2383.716 2326.0605
20 -0.45201474 2665.7727 4189.1953

Total number of rows: 15247

Table truncated, full table size 512 Kbytes.




Supplementary data files not provided

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