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Sample GSM159329 Query DataSets for GSM159329
Status Public on Mar 01, 2007
Title HepG2_Sb rep3
Sample type RNA
 
Source name Hep G2 treated with Bis [(+)-tartrato] diantimonate (III) dipotassium trihydrate
Organism Homo sapiens
Characteristics Cell bank no: RCB1648
Cell name: Hep G2
Sex: male
Age of sampling: 15 years
Tissue derived: liver
Case history: hepatocyte carcinoma
Life span: infinite
Classification: Transformed
Biomaterial provider RIKEN BRC CELL BANK
Treatment protocol Cells were grown to 70% confluency in 60 mm culture dishes and exposed to 200 uM Bis [(+)-tartrato] diantimonate (III) dipotassium trihydrate for 6h at 37 °C.
Growth protocol Cells were cultured in Eagle's minimal essential medium (MEM) (Nissui, Tokyo, Japan) supplemented with 1% non-essential amino acid (Invitrogen, Carlsbad, CA), 10% fetal bovine serum and 60 mg/ml kanamycin at 37 °C and 5% CO2.
Extracted molecule total RNA
Extraction protocol The cells were were washed with phosphate buffered saline (PBS) and lysed directly on culture dishes. Total RNA was extracted using RNeasy Mini Kit (Qiagen, Hilden, Germany).
Label biotin
Label protocol Target preparation was performed according to One-Cycle Eukaryotic Target Labeling Assay protocols described in Affymetrix technical manual (Affymetrix, Santa Clara, CA). cDNA was synthesized from the 5 ug of total RNA by using One-Cycle cDNA Synthesis kit (Invitrogen, Carlsbad, CA) with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. cRNA was synthesized from the cDNA and biotin-labeled by in vitro transcription using IVT Labeling kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol Target preparation and hybridization was performed according to One-Cycle Eukaryotic Target Labeling Assay protocols described in Affymetrix technical manual (Affymetrix, Santa Clara, CA). Labeled cRNA was fragmented by incubation at 94 °C for 35 min in the presence of 40 mM Tris acetate, pH 8.1, 100 mM potassium acetate, and 30 mM magnesium acetate. Ten ug of fragmented cRNA was hybridized to a Human Genome Focus array (Affymetrix, Santa Clara, CA) containing probes for 8795 human genes for 16 h at 45 °C. After hybridization, the microarrays were automatically washed and stained with streptavidin-phycoerythrin by using a fluidics station 450 (Affymetrix, Santa Clara, CA).
Scan protocol Probe arrays were scanned with the Genechip System confocal scanner (Affymetrix, Santa Clara, CA).
Description Gene expression data from Sb treated Hep G2 cells
Data processing The data were analyzed with MAS5 using Avadis 4.2 prophetic (Strand Genomics, Redwood City, CA).
 
Submission date Jan 30, 2007
Last update date Feb 02, 2007
Contact name Akinobu Ito
E-mail(s) [email protected]
Phone +81-11-706-7588
Fax +81-11-706-7588
Organization name Hokkaido University
Department Graduate School of Engineering
Lab Water Quality Control Engineering
Street address North-13, West-8, Kitaku
City Sapporo
ZIP/Postal code 060-8628
Country Japan
 
Platform ID GPL201
Series (1)
GSE6907 Gene expression changes induced by heavy metals and other chemicals

Data table header descriptions
ID_REF
VALUE MAS5-calculated signal intensity
ABS_CALL the call in an absolute analysis: (P)present, (A)absent, (M)marginal
DETECTION P-VALUE detection p-value

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
1007_s_at 674.6069 P 0.004862762
1053_at 273.36554 P 0.003584867
117_at 15652.262 P 0.000218889
121_at 647.22925 P 0.004862762
1255_g_at 10.396073 A 0.7810167
1294_at 149.85095 A 0.117160484
1316_at 128.13757 P 0.031335693
1320_at 133.23277 A 0.28474715
1431_at 16.412886 A 0.8103525
1438_at 19.9615 A 0.7810167
1487_at 572.6083 P 0.009985438
1494_f_at 197.89404 M 0.054470435
1598_g_at 86.09481 A 0.45881578
160020_at 284.9333 P 0.024710983
1729_at 169.97214 A 0.081336655
177_at 187.82065 P 0.019303527
1773_at 146.65388 A 0.107300945
1861_at 169.86026 A 0.12760554
200000_s_at 1742.3004 P 0.000244141
200001_at 2084.101 P 0.000244141

Total number of rows: 8793

Table truncated, full table size 279 Kbytes.




Supplementary file Size Download File type/resource
GSM159329.CEL.gz 698.2 Kb (ftp)(http) CEL

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