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Sample GSM1380962 Query DataSets for GSM1380962
Status Public on May 07, 2014
Title Bl6 WT P14_2
Sample type RNA
 
Source name Day 3 post LCMV infection sorted P14 cells from the spleen
Organism Mus musculus
Characteristics tissue: spleen
nk depletion: no
genetic background: Bl6
genotype: WT
treatment: none
Treatment protocol naïve Bl6 mice were depleted of NK cells using the aNK1.1 depleting antibody or left untreated, followed by co-transfer of WT and Ifnar1-/- P14 cells. One day later the mice were infected with LCMV8.7 + Vaccinia Virus-G2. At day 3 post infection WT and Ifnar1-/- P14 cells were FACS sorted to purity, frozen and shipped to Miltenyi Biotec for microarray analysis
Extracted molecule total RNA
Extraction protocol RNA was extracted using standard protocols (NucleoSpin RNA II)
Label Cy3
Label protocol Cy3 labelling was achieved using the Agilent low input quick Amp labeling kit (Agilent Technologies)
 
Hybridization protocol Hybridization was performed according to the Agilent 60-mer oligo microarray processing protocol using the Agilent Gene Expression Hybridization Kit. 600ug Cy3-labeled fragmented cRNA in hybridization buffer was hybridized overnight to Agilent Whole Mouse Genome Oligo Microarrays 8x60K using Agilents recommended hybridization chamber and oven. The microarrays were washed once with the Agilent Gene Expression Wash Buffer 1 for 1 min at room temperature followed by a second wash with preheated Agilent Gene expression wash buffer 2 (37 °C) for 1 min. The last washing step was performed with acetonitrile.
Scan protocol Flourescene signals of the hybridized Agilent Microarrays were detected using Agilent`s Microarray Scanner System.
Data processing Agilent Feature Extraction Software was use to read out and process the microarray image files.
 
Submission date May 06, 2014
Last update date May 07, 2014
Contact name Annette Oxenius
E-mail(s) [email protected]
Organization name ETH Zurich
Department Microbiology
Lab Oxenius
Street address Vladimir-Prelog-weg 1-5/10
City Zurich
ZIP/Postal code 8093
Country Switzerland
 
Platform ID GPL13912
Series (1)
GSE57355 The effect of type-I interferon signaling directly on CD8+ T cells following LCMV infection in the presence or absence of NK cells.

Data table header descriptions
ID_REF
VALUE Agilent Feature Extraction default normalized signal

Data table
ID_REF VALUE
4 0.451166
5 1.355937
6 0.447726
7 0.445868
8 5.85394
9 0.44267
10 0.441182
11 0.439898
12 0.438362
13 8.165807
14 340.335241
15 0.434578
16 0.433286
17 268.097967
18 16.497872
19 130.294493
20 5073.551713
21 11.341719
22 1.768979
23 62.975057

Total number of rows: 59305

Table truncated, full table size 880 Kbytes.




Supplementary file Size Download File type/resource
GSM1380962_252800512384_S01_GE1_107_Sep09_1_3.txt.gz 11.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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