NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM147099 Query DataSets for GSM147099
Status Public on Dec 01, 2006
Title Actinomycin D treated A549 human lung cancer cell cultures replicate A
Sample type RNA
 
Source name Actinomycin D treated A549 human lung cancer cell cultures replicate A
Organism Homo sapiens
Characteristics A549 human lung cancer cells (1X10^5 per T-25 flask in 7 mL complete RPMI 1640 medium) were seeded eights days prior to treatment of non-cycling plateau phase cultures with drug. At four hours prior to RNA isolation, actinomycin D (5 ug/mL final concentration) was added to the culture. After incubation for four hours, the culture was washed twice with HBSS supplemented with 0.5% BSA and total RNA was isolated.
Biomaterial provider ATCC
Treatment protocol A549 human lung cancer cells (1X10^5 per T-25 flask in 7 mL complete RPMI 1640 medium) were seeded eights days prior to treatment of non-cycling plateau phase cultures with drug. At four hours prior to RNA isolation, actinomycin D (5 ug/mL final concentration) was added to the culture. After incubation for four hours, the culture was washed twice with HBSS supplemented with 0.5% BSA and total RNA was isolated.
Growth protocol A549 human lung cancer cells (1X10^5 per T-25 flask in 7 mL complete RPMI 1640 medium) were seeded eights days prior to treatment of non-cycling plateau phase cultures with drug. At four hours prior to RNA isolation, actinomycin D (5 ug/mL final concentration) was added to the culture. After incubation for four hours, the culture was washed twice with HBSS supplemented with 0.5% BSA and total RNA was isolated.
Extracted molecule total RNA
Extraction protocol We used the RNA Stat-60 reagent (Tel-Test, Inc.) according to the manufacturer's recomended protocols.
Label Affymetrix single-stage biotin
Label protocol We used GeneChip® One-Cycle Target Labeling and Control Reagents according to the manufacturer's recomended protocols.
 
Hybridization protocol We used the Affymetrix Hybridization Oven 640 and GeneChip® Fluidics Station 450 according to the manufacturer's recomended protocols.
Scan protocol We used the Affymetrix GeneChip® Scanner 3000 according to the manufacturer's recomended protocols.
Description A549 human lung cancer cells (1X10^5 per T-25 flask in 7 mL complete RPMI 1640 medium) were seeded eights days prior to treatment of non-cycling plateau phase cultures with drug. At four hours prior to RNA isolation, actinomycin D (5 ug/mL final concentration) was added to the culture. After incubation for four hours, the culture was washed twice with HBSS supplemented with 0.5% BSA and total RNA was isolated.
Data processing RMA Normalization
 
Submission date Nov 25, 2006
Last update date Aug 28, 2018
Contact name Joseph Gerard Hacia
E-mail(s) hacia@hsc.usc.edu
Phone 323-442-3030
Organization name University of Southern California
Department Biochemistry and Molecular Biology
Lab Hacia Lab
Street address 2250 Alcazar Street, IGM 261
City Los Angeles
State/province CA
ZIP/Postal code 90089
Country USA
 
Platform ID GPL570
Series (1)
GSE6400 Cultured A549 lung cancer cells treated with actinomycin D and sapphyrin PCI-2050
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE Processed_Signal_Using_RMA

Data table
ID_REF VALUE
1007_s_at 1082.19
1053_at 239.75
117_at 42.89
121_at 224.37
1255_g_at 19.4
1294_at 58.66
1316_at 62.9
1320_at 54.79
1405_i_at 19.99
1431_at 37.64
1438_at 55.1
1487_at 263.36
1494_f_at 66.27
1552256_a_at 906.46
1552257_a_at 184.94
1552258_at 38.4
1552261_at 52.36
1552263_at 28.85
1552264_a_at 159.08
1552266_at 22.61

Total number of rows: 54675

Table truncated, full table size 909 Kbytes.




Supplementary file Size Download File type/resource
GSM147099.CEL.gz 4.6 Mb (ftp)(http) CEL

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