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Search results for the GEO ID: GSE8066
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GPL ID
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Title
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Description
Characteristics
GSM199428
GPL570
SKNAS-NmycER, t=0 SKNAS-NmycER cells Cell line from neuroblastoma tumor, stably transfected with NmycER expression vector. SKNAS-NmycER cells were grown under standard conditions and harvested at diferent timepoints after addition of 4-hydroxytamoxifen. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199429
GPL570
SKNAS-NmycER, t=24 hrs SKNAS-NmycER cells Cell line from neuroblastoma tumor, stably transfected with NmycER expression vector SKNAS-NmycER cells were grown under standard conditions and harvested at diferent timepoints after addition of 4-hydroxytamoxifen. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199430
GPL570
SKNAS-NmycER, t=72 hrs SKNAS-NmycER cells Cell line from neuroblastoma tumor, stably transfected with NmycER expression vector. SKNAS-NmycER cells were grown under standard conditions and harvested at diferent timepoints after addition of 4-hydroxytamoxifen. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199431
GPL570
SKNAS-NmycER, t=144 hrs SKNAS-NmycER cells Cell line from neuroblastoma tumor, stably transfected with NmycER expression vector. SKNAS-NmycER cells were grown under standard conditions and harvested at diferent timepoints after addition of 4-hydroxytamoxifen. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199432
GPL570
IMR32-DKK1 c63, t=0 IMR32-DKK1 c63 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199433
GPL570
IMR32-DKK1 c63, t=24 hrs IMR32-DKK1 c63 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199434
GPL570
IMR32-DKK1 c63, t=72 hrs IMR32-DKK1 c63 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199435
GPL570
IMR32-DKK1 c63, t=288 hrs IMR32-DKK1 c63 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199436
GPL570
IMR32-DKK1 c66, t=0 IMR32-DKK1 c66 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199437
GPL570
IMR32-DKK1 c66, t=24 hrs IMR32-DKK1 c66 Cell line from a neuroblastoma tumor, stably transfected with an inducible MYCN expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199441
GPL570
IMR32-DKK1 c66, t=72 hrs IMR32-DKK1 c66 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199442
GPL570
IMR32-DKK1 c66, t=288 hrs IMR32-DKK1 c66 Cell line from a neuroblastoma tumor, stably transfected with an inducible DKK1 expression vector IMR32-DKK1 cells were grown under standard conditions. Cells were harvested, at 70% confluency, at different time points after adding doxycyclin. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199473
GPL570
SHEP-21N, t=0 SHEP-21N Cell line from a neuroblastoma tumor, stably transfected with an inducible MYCN expression vector SHEP-21N cells were grown under standard conditions in presence of tetracycline (no MYCN expression) for two weeks. Tetracyclin was washed away and cells were harvested, at 70% confluency, at different time points after tetracycline removal. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199474
GPL570
SHEP-21N, t=8 hrs SHEP-21N Cell line from a neuroblastoma tumor, stably transfected with an inducible MYCN expression vector SHEP-21N cells were grown under standard conditions in presence of tetracycline (no MYCN expression) for two weeks. Tetracyclin was washed away and cells were harvested, at 70% confluency, at different time points after tetracycline removal. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199475
GPL570
SHEP-21N, t=24 hrs SHEP-21N Cell line from a neuroblastoma tumor, stably transfected with an inducible MYCN expression vector SHEP-21N cells were grown under standard conditions in presence of tetracycline (no MYCN expression) for two weeks. Tetracyclin was washed away and cells were harvested, at 70% confluency, at different time points after tetracycline removal. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
GSM199479
GPL570
SHEP-21N, t=120 hrs SHEP-21N Cell line from a neuroblastoma tumor, stably transfected with an inducible MYCN expression vector SHEP-21N cells were grown under standard conditions in presence of tetracycline (no MYCN expression) for two weeks. Tetracyclin was washed away and cells were harvested, at 70% confluency, at different time points after tetracycline removal. Total RNA was isolated and analyzed on Affymetrix U133 Plus 2.0.
 
 
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