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Search results for the GEO ID: GSE1455
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GSM ID
GPL ID
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Title
Source name
Description
Characteristics
GSM24493
GPL96
RHE2_T1_R1, Control Monolayer Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24494
GPL96
RHE2_T1_R2, Control Monolayer Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24495
GPL96
RHE2_T1_R3, Control Monolayer Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24496
GPL96
RHE2_T2_R1, Spheroid prior to storage Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24497
GPL96
RHE2_T2_R2, Spheroid prior to storage Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24498
GPL96
RHE2_T2_R3, Spheroid prior to storage Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24499
GPL96
RHE2_T3_R1, 0 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24500
GPL96
RHE2_T3_R2, 0 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24501
GPL96
RHE2_T3_R3, 0 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24502
GPL96
RHE2_T4_R1, 6 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24503
GPL96
RHE2_T4_R2, 6 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24504
GPL96
RHE2_T4_R3, 6 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24505
GPL96
RHE2_T5_R1, 24 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24506
GPL96
RHE2_T5_R2, 24 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24507
GPL96
RHE2_T5_R3, 24 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24508
GPL96
RHE2_T6_R1, 72 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24509
GPL96
RHE2_T6_R2, 72 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
GSM24510
GPL96
RHE2_T6_R3, 72 hr recovery Kidney 293 HEK Cells 60-70% confluent Human embryonic kidney cell were split into suspension overagarose to form spheroids and grown for an additional 4 days insuspension over agarose prepared with 10% FBS supplemented DMEM Following growth, media was removed and the spheroids were stored on thesurface of the agarose in vacuum sealed flasks for a 2 week interval at roomtemperature in the dark. The samples were compared against unstored controls of both spheroids andmonolayer (at 60-70% confluence)samples. All samples were conducted intriplicate. Rehydration was conducted with DMEM (Invitrogen) containing 10%FBS up tothe final 72hr rehydration timepoint.
 
 
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