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Sample GSM1172667 Query DataSets for GSM1172667
Status Public on Jun 22, 2013
Title M1, NS1 M106I 3
Sample type RNA
 
Source name M1, NS1 M106I
Organism Mus musculus
Characteristics cell line: M1
cell type: immortal kidney epithilium
Treatment protocol Confluent monolayers of 1.5E6 M1 cells in 35 mm dishes were infected with rHK-wt or rHK NS mutant viruses (MOI = 2) or mock-infected with PBS in triplicate for n=3 biological replicates before overflay with 3 ml of MEM.
Growth protocol M1 cells (Mouse kidney epithelium; ATCC, CRL-2038) were maintained in minimum essential medium (MEM). MEM was supplemented with L-glutamine (2 mM), Penicillin (100 U/ml), Streptomycin (100 ug/ml) and fetal bovine serum (FBS) (10%). All cells were incubated at 37°C in the presence of 5% CO2.
Extracted molecule total RNA
Extraction protocol At 8 hpi, the cellular RNA was collected using manufacturer’s protocol (QIAGEN RNeasy mini-kit) quantified using a PowerWave XS2, Microplate Spectrophotometer (BioTek Instruments, Inc. Winooski, VT, United States).
Label Biotin
Label protocol Sense strand target cDNA were prepared using the Ambion WT Expression kit (Life Technologies cat# 4411973/4) from 300 ng of total RNA. Fragmentation and labeling were performed according to the standard Affymetrix protocol from 5.5 ug of cDNA (Genechip WT Terminal Labeling and Hybridization Manual Rev.7, Affymetrix).
 
Hybridization protocol Target cDNA were hybridized to the Mouse Gene 1.0 ST array according to Affymetrix standard protocol (Genechip WT Terminal Labeling and Hybridization Manual Rev.7, Affymetrix). GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix Genechip Scanner 3000 7G.
Description Affy#4483_1.0: biological replicate 3
Data processing RMA normalization and scaling of data was performed with Affymetrix Expression Console v. 1.2
 
Submission date Jun 21, 2013
Last update date Jun 22, 2013
Contact name Earl Garnet Brown
E-mail(s) ebrown@uottawa.ca
Phone 613 224 7533
Organization name University of Ottawa
Department Biochemistry Microbiology and Immunology
Lab RGN 4109
Street address 451 Smyth Rd
City Ottawa
State/province Ontario
ZIP/Postal code KIH 8M5
Country Canada
 
Platform ID GPL6246
Series (2)
GSE48200 Influenza A/Hong Kong/156/1997(H5N1) virus NS1 gene mutations F103L and M106I both increase IFN antagonism, virulence and cytoplasmic localization but differ in binding to RIG-I and CPSF30
GSE48217 Identification of Adaptive mutations in the influenza A virus non-structural 1 gene that increase cytoplasmic localization and differentially regulate host gene expression

Data table header descriptions
ID_REF
VALUE Log2 RMA Signal

Data table
ID_REF VALUE
10338001 10.6022
10338002 6.18754
10338003 8.84389
10338004 6.26436
10338005 2.0014
10338006 2.30789
10338007 2.77028
10338008 3.6384
10338009 7.99415
10338010 2.06905
10338011 5.66045
10338012 2.1549
10338013 1.86821
10338014 1.92165
10338015 1.86493
10338016 7.42603
10338017 11.7092
10338018 6.69088
10338019 5.09279
10338020 7.95835

Total number of rows: 35557

Table truncated, full table size 586 Kbytes.




Supplementary file Size Download File type/resource
GSM1172667_Affy_4483_1.0_MoGene-1_0-st-v1_.CEL.gz 4.1 Mb (ftp)(http) CEL
GSM1172667_Affy_4483_1.0_MoGene-1_0-st-v1_.rma-gene-default.chp.gz 270.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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