NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1172641 Query DataSets for GSM1172641
Status Public on Jun 22, 2013
Title A549, NS1 F103L 1
Sample type RNA
 
Source name A549, NS1 F103L
Organism Homo sapiens
Characteristics cell line: A549
cell type: lung epithilium
Treatment protocol Confluent monolayers of 1.5E6 A549 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 fro 8 h at 37 C.
Growth protocol A549 cells (ATCC) 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 250 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 Human 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#4348_1.0: biological replicate 1
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 GPL6244
Series (1)
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

Data table header descriptions
ID_REF
VALUE Log2 RMA Signal

Data table
ID_REF VALUE
7892501 0.596247
7892502 3.34994
7892503 1.19212
7892504 7.80677
7892505 1.25101
7892506 3.08756
7892507 3.75526
7892508 1.08696
7892509 9.80925
7892510 1.42329
7892511 1.87491
7892512 6.05589
7892513 1.04894
7892514 9.46842
7892515 8.13687
7892516 1.10671
7892517 4.06451
7892518 1.51211
7892519 2.83085
7892520 7.47858

Total number of rows: 33297

Table truncated, full table size 517 Kbytes.




Supplementary file Size Download File type/resource
GSM1172641_Affy_4348_1.0_HuGene-1_0-st-v1_.CEL.gz 3.5 Mb (ftp)(http) CEL
GSM1172641_Affy_4348_1.0_HuGene-1_0-st-v1_.rma-gene-default.chp.gz 256.0 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap