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Search results for the GEO ID: GSE12056
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GSM ID
GPL ID
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Title
Source name
Description
Characteristics
GSM304303
GPL570
K562 cells control replicate 1 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. None
GSM304304
GPL570
K562 cells control replicate 2 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. None
GSM304479
GPL570
K562 cells control replicate 3 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304480
GPL570
K562 cells control replicate 5 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304481
GPL570
K562 cells control replicate 6 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304482
GPL570
K562 cells control replicate 7 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304483
GPL570
K562 cells control replicate 8 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304484
GPL570
K562 cells control replicate 9 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304486
GPL570
K562 cells control replicate 10 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days none
GSM304487
GPL570
K562 cells CREB Knock-out replicate 1 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304488
GPL570
K562 cells CREB Knock-out replicate 2 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. . The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304489
GPL570
K562 cells CREB Knock-out replicate 3 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304490
GPL570
K562 cells CREB Knock-out replicate 4 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304491
GPL570
K562 cells CREB Knock-out replicate 5 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304492
GPL570
K562 cells CREB Knock-out replicate 6 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. . The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304493
GPL570
K562 cells CREB Knock-out replicate 7 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304494
GPL570
K562 cells CREB Knock-out replicate 8 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304495
GPL570
K562 cells CREB Knock-out replicate 9 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304496
GPL570
K562 cells CREB Knock-out replicate 10 K562 cells CREB Knock-out K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. The CREB specific shRNA sequences were selected and validated based on accepted parameters established by Tuschl et al. none
GSM304498
GPL570
K562 cells control replicate 4 K562 cells K562 (Iscoves + 10% FCS) and TF-1 (RPMI + 10%FCS + rhGM-CSF. Cells were cultured at 37oC, 5% CO2 and split every 3 to 4 days. None
 
 
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