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Sample GSM1366504 Query DataSets for GSM1366504
Status Public on Sep 01, 2014
Title Ly49G+ NK cells_rep3
Sample type RNA
 
Source name IL2 cultured splenocytes_Ly49G+
Organism Mus musculus
Characteristics strain: C57BL/5
tissue: Spleen
cell type: natural killer
Growth protocol Splenocytes were removed from C57BL/6 mice and were then incubated with antibodies against Thy1.2 and rabbit complement to eliminate T cells and were then cultured in media and 1000 IU IL-2 for 7 days.
Extracted molecule total RNA
Extraction protocol Flow cytometric cell sorting was performed by gating on CD3-CD122+Ly49G2+Ly49C/I- versus CD3-CD122+Ly49G2-Ly49C/I+. Total mRNA was extracted using the Qiagen RNeasy kit. RNA quality was checked on an Agilent Bioanalyzer. All samples used for microarray analysis had a high quality score (RIN >9). 100 ng of RNA was reverse transcribed and amplified using the Ambion WT expression kit following manufacturer’s suggested protocol.
Label Biotin
Label protocol Sense strand cDNA was fragmented and labeled using Affymetrix WT terminal labeling kit.
 
Hybridization protocol Three replicates of each group were hybridized to Affymetrix mouse Gene ST 1.0 GeneChip in Affymetrix hybridization oven at 45C, 60rpm for 16 hrs.
Scan protocol Wash and stain were performed on Affymetrix Fluidics Station 450 and scanned on Affymetrix GeneChip scanner 3000.
Description IL2 cultured splenocytes sorted for Ly49G expression
Data processing Data were collected using Affymetrix AGCC software. Statistical and clustering analysis was performed with Partek Genomics Suite software using the RMA normalization algorithm. Differentially expressed genes were identified with ANOVA analysis. Genes that were up- or down-regulated more than 1.5 fold and with a p<0.001 were considered significant. Significant genes were analyzed for enrichment for pathways using DAVID bioinformatics database (http://david.abcc.ncifcrf.gov/) and Ingenuity Pathway Analysis software.
Quantile normalized gene level expression values from GeneBASE
 
Submission date Apr 09, 2014
Last update date Sep 01, 2014
Contact name Stephen Kent Anderson
E-mail(s) [email protected]
Phone 301-846-1330
Organization name NCI-Frederick
Department CCR
Lab Experimental Immunology
Street address Building 560, room 31-33
City Frederick
State/province MD
ZIP/Postal code 21702-1201
Country USA
 
Platform ID GPL10740
Series (1)
GSE56662 Expression data from murine natural killer cell subsets based on Ly49 receptor expression in C57BL/6 mice (C/I+ versus Ly49G2+ NK cells)

Data table header descriptions
ID_REF
VALUE RMA Normalized signal

Data table
ID_REF VALUE
10338001 11.68
10338002 7.74
10338003 10.11
10338004 8.39
10338005 4.02
10338006 4.3
10338007 4.65
10338008 5.27
10338009 9.63
10338010 4.05
10338011 7.07
10338012 4.18
10338013 3.85
10338014 3.9
10338015 3.87
10338016 8.96
10338017 12.61
10338018 8.18
10338019 6.63
10338020 9.52

Total number of rows: 241576

Table truncated, full table size 3327 Kbytes.




Supplementary file Size Download File type/resource
GSM1366504_G2+_3_MoGene-1_0-st-v1.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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