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Sample GSM1172663 Query DataSets for GSM1172663
Status Public on Jun 22, 2013
Title M1, NS1 M106V 2
Sample type RNA
 
Source name M1, NS1 M106V
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#4443_1.0: biological replicate 2
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 10.9561
10338002 6.38999
10338003 9.26987
10338004 6.33082
10338005 2.0406
10338006 2.34275
10338007 2.83252
10338008 3.754
10338009 8.34221
10338010 2.08703
10338011 5.74385
10338012 2.18699
10338013 1.86757
10338014 1.93604
10338015 1.90194
10338016 7.66603
10338017 11.8608
10338018 6.83717
10338019 5.23734
10338020 8.25661

Total number of rows: 35557

Table truncated, full table size 586 Kbytes.




Supplementary file Size Download File type/resource
GSM1172663_Affy_4443_1.0_MoGene-1_0-st-v1_.CEL.gz 4.0 Mb (ftp)(http) CEL
GSM1172663_Affy_4443_1.0_MoGene-1_0-st-v1_.rma-gene-default.chp.gz 270.7 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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