NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3357304 Query DataSets for GSM3357304
Status Public on Aug 28, 2018
Title clone8_45min_rep1
Sample type RNA
 
Source name Murine L929 cells, reovirus strain clone8-infected, 45min after actinomycin D treatment
Organism Mus musculus
Characteristics cell line: fibroblast cell line L929
infection: reovirus strain clone8-infected
agent: actinomycin D
time: 45min
Treatment protocol L929 cells were plated in 150 x 25 mm tissue culture plates and were allowed to incubate at 37oC for 4 h, after which time the medium was removed and cells were mock-infected or infected with purified virions (Dearing, c87 or c8) at a multiplicity of infection of 80 plaque forming units/cell. After a 1.5 h viral adsorption at 37C, medium was added and samples were incubated at 37oC for an additional 18 h. At 19.5 h post-infection, actinomycin D was added at a final concentration of 10 µg/ml to stop transcription.
Growth protocol Murine L929 cells were maintained as suspension cultures as described previously
Extracted molecule total RNA
Extraction protocol Total RNA was isolated at 0, 45, 90 and 120 min post-actinomycin D treatment using Trizol reagent according to the manufacturer’s instructions. Total RNA was purified with the RNeasy column.
Label biotin
Label protocol The purified cDNA was used for an in vitro transcription reaction using T7 RNA polymerase and biotinylated nucleotides following the manufacturer’s protocol.
 
Hybridization protocol Biotinylated anti-sense cRNA was purified with the RNeasy column; 15 µg was fragmented according to Affymetrix instructions’ and hybridized to Affymetrix murine U74Av2 oligonucleotide microarrays.
Scan protocol Microarrays were scanned on a Hewlett Packard Agilent 2200 confocal scanner.
Description Gene expression data from reovirus strain clone 8-infected cells 45min after adding actinomycin D
Data processing Normalized signal intensities were obtained using Affymetrix MAS 5.0 software as described previously
 
Submission date Aug 27, 2018
Last update date Aug 28, 2018
Contact name Liang Guo
Organization name University of Minnesota
Street address 2001 6th Street SE
City minneapolis
State/province MINNESOTA
ZIP/Postal code 55455
Country USA
 
Platform ID GPL81
Series (1)
GSE119061 Reovirus infection induces stabilization and up-regulation of cellular transcripts that encode regulators of TGF-beta signaling

Data table header descriptions
ID_REF
VALUE MAS5.0 Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-MurIL2_at 4.06984 A 0.868639
AFFX-MurIL10_at 3.48388 A 0.712257
AFFX-MurIL4_at 7.53162 A 0.39692
AFFX-MurFAS_at 9.14775 A 0.5
AFFX-BioB-5_at 95.6997 P 0.00401721
AFFX-BioB-M_at 144.324 P 5.16732e-05
AFFX-BioB-3_at 71.1117 P 0.000445901
AFFX-BioC-5_at 232.904 P 0.000169227
AFFX-BioC-3_at 175.141 P 5.16732e-05
AFFX-BioDn-5_at 220.13 P 8.13208e-05
AFFX-BioDn-3_at 1053.29 P 0.00010954
AFFX-CreX-5_at 2299.64 P 4.42873e-05
AFFX-CreX-3_at 3271.68 P 4.42873e-05
AFFX-BioB-5_st 6.13232 A 0.382599
AFFX-BioB-M_st 15.8903 A 0.58862
AFFX-BioB-3_st 6.88353 A 0.672921
AFFX-BioC-5_st 3.01841 A 0.824672
AFFX-BioC-3_st 1.14374 A 0.824672
AFFX-BioDn-5_st 41.3315 A 0.0894781
AFFX-BioDn-3_st 45.7426 P 0.0309764

Total number of rows: 12488

Table truncated, full table size 364 Kbytes.




Supplementary file Size Download File type/resource
GSM3357304_clone8_45min_1.CEL.gz 2.8 Mb (ftp)(http) CEL
GSM3357304_clone8_45min_1.CHP.gz 4.5 Mb (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