NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3308605 Query DataSets for GSM3308605
Status Public on Jul 28, 2018
Title A498 DGAT1/2 shRNA cells, vehicle treatment, normoxia, biol repl 1
Sample type RNA
 
Source name A498 expressing non-induced DGAT1/2 shRNA construct grown under serum deprivation and normoxia
Organism Homo sapiens
Characteristics treatment: vehicle
cell line: A498
cell type: Clear cell renal cell carcinoma (ccRCC)
genotype/variation: wildtype
oxygen levels: normoxia
Treatment protocol Vehicle/Doxycycline treatment was applied for 5 days and normoxic/hypoxic treatment was applied for 2 days before RNA extraction
Growth protocol Low serum growth conditions. Vehicle/Doxycycline treatment was applied for 5 days and normoxic/hypoxic treatment was applied for 2 days before RNA extraction
Extracted molecule total RNA
Extraction protocol total RNA extraction was performed with RNEasy columns according to the manufacturer's instructions
Label biotin
Label protocol 250ng of total RNA was converted to biotinylated cDNA using standard protocols used by the Molecular Profiling Core at the University of Pennsylvania
 
Hybridization protocol Five and a half micrograms of labeled cDNA were added to Affymetrix hybridization cocktails, heated at 99ºC for 5 min and hybridized for 16 h at 45ºC to Human Transcriptome 2.0 ST GeneChips (Affymetrix Inc., Santa Clara CA) using the GeneChip Hybridization oven 645. The microarrays were then washed at low (6X SSPE) and high (100mM MES, 0.1M NaCl) stringency and stained with streptavidin-phycoerythrin. Fluorescence was amplified by adding biotinylated anti-streptavidin and an additional aliquot of streptavidin-phycoerythrin stain.
Scan protocol A GeneChip 3000 7G scanner was used to collect fluorescence signal.
Data processing RMA-sst was applied using Affymetroix Transcriptome Analysis Console (TAC) with default settings
 
Submission date Jul 27, 2018
Last update date Jul 28, 2018
Contact name Daniel Ackerman
E-mail(s) [email protected]
Phone 2155739755
Organization name University of Pennsylvania
Street address 421 Curie Blvd, BRB II/III, Rm 646
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platform ID GPL17586
Series (1)
GSE117775 Effect of DGAT loss on hypoxic tumor cells growing under serum-deprived conditions

Data table header descriptions
ID_REF
VALUE log2-transformed normalized expression as output from TAC

Data table
ID_REF VALUE
2824546_st 18.9987
2824549_st 17.4768
2824551_st 17.4549
2824554_st 17.3593
2827992_st 16.4952
2827995_st 17.3578
2827996_st 16.1525
2828010_st 12.903
2828012_st 16.6131
2835442_st 15.8344
2835447_st 12.2249
2835453_st 11.8434
2835456_st 17.655
2835459_st 14.6141
2835461_st 13.9584
2839509_st 16.7684
2839511_st 13.7403
2839513_st 16.3392
2839515_st 13.6163
2839517_st 16.0148

Total number of rows: 70523

Table truncated, full table size 1655 Kbytes.




Supplementary file Size Download File type/resource
GSM3308605_5336_61634_SVN1_HTA_2.0st.CEL.gz 25.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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