Nice View of CleanEx Exp : GSE1302E_DOC

[General] [References] [Expression data]

General information about the entry
Dataset code GSE1302E
Dataset Title primary trophoblast study
Description Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA..
Organism Homo sapiens
Format Type Intensity
Affymetrix;HG-U95E
Number of Experiments 15
Maximum log 9.6385670056459
Minimum log -6.50095691234691
References
Original URL http://www.ncbi.nlm.nih.gov/projects/geo/query/acc.cgi?acc=GSE1302
Paper Reference Mecham BH et al. Physiol Genomics. 2004 Aug 11;18(3):308-15.
MEDLINE Reference 15161964
Experiments
Experiment numberExperiment CodeExperiment Description
1GSE1302E_GSM2158195e Control_1;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with DMSO as a vehicle control. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 1, replicate 1"; CrossRefs: GSE1302A_EX1 GSE1302B_EX1 GSE1302C_EX1 GSE1302D_EX1;
2GSE1302E_GSM2158295e Control_2;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with DMSO as a vehicle control. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 1, replicate 2"; CrossRefs: GSE1302A_EX2 GSE1302B_EX2 GSE1302C_EX2 GSE1302D_EX2;
3GSE1302E_GSM2158395e Control_3;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with DMSO as a vehicle control. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 1, replicate 3"; CrossRefs: GSE1302A_EX3 GSE1302B_EX3 GSE1302C_EX3 GSE1302D_EX3;
4GSE1302E_GSM2158495e Control_4;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with DMSO as a vehicle control. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 1, replicate 4"; CrossRefs: GSE1302A_EX4 GSE1302B_EX4 GSE1302C_EX4 GSE1302D_EX4;
5GSE1302E_GSM2158595e Control_5;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with DMSO as a vehicle control. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 1, replicate 5"; CrossRefs: GSE1302A_EX5 GSE1302B_EX5 GSE1302C_EX5 GSE1302D_EX5;
6GSE1302E_GSM2158695e Troglitazone_1;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 10 uM Troglitazone . RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 2, replicate 1"; CrossRefs: GSE1302A_EX6 GSE1302B_EX6 GSE1302C_EX6 GSE1302D_EX6;
7GSE1302E_GSM2158795e Troglitazone_2;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 10 uM Troglitazone . RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 2, replicate 2"; CrossRefs: GSE1302A_EX7 GSE1302B_EX7 GSE1302C_EX7 GSE1302D_EX7;
8GSE1302E_GSM2158895e Troglitazone_3;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 10 uM Troglitazone . RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 2, replicate 3"; CrossRefs: GSE1302A_EX8 GSE1302B_EX8 GSE1302C_EX8 GSE1302D_EX8;
9GSE1302E_GSM2158995e Troglitazone_4;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 10 uM Troglitazone . RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 2, replicate 4"; CrossRefs: GSE1302A_EX9 GSE1302B_EX9 GSE1302C_EX9 GSE1302D_EX9;
10GSE1302E_GSM2159095e Troglitazone_5;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 10 uM Troglitazone . RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 2, replicate 5"; CrossRefs: GSE1302A_EX10 GSE1302B_EX10 GSE1302C_EX10 GSE1302D_EX10;
11GSE1302E_GSM2159195e GW7845_1;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 3, replicate 1"; CrossRefs: GSE1302A_EX11 GSE1302B_EX11 GSE1302C_EX11 GSE1302D_EX11;
12GSE1302E_GSM2159295e GW7845_2;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 3, replicate 2"; CrossRefs: GSE1302A_EX12 GSE1302B_EX12 GSE1302C_EX12 GSE1302D_EX12;
13GSE1302E_GSM2159395e GW7845_3;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 3, replicate 3"; CrossRefs: GSE1302A_EX13 GSE1302B_EX13 GSE1302C_EX13 GSE1302D_EX13;
14GSE1302E_GSM2159495e GW7845_4;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 3, replicate 4"; CrossRefs: GSE1302A_EX14 GSE1302B_EX14 GSE1302C_EX14 GSE1302D_EX14;
15GSE1302E_GSM2159595e GW7845_5;Primary cultures of human trophoblasts were established from normal, term placenta. Cells were treated five hours after plating. This sample was treated with 1 uM GW7845. RNA was extracted after 48 hours of treatment using Tri-reagent. Each sample was pooled from three individual placentas prior to target generation. Targets were produced using standard Affymetrix procedures from 30ug of total RNA. This sample is also known as Treatment 3, replicate 5"; CrossRefs: GSE1302A_EX15 GSE1302B_EX15 GSE1302C_EX15 GSE1302D_EX15;