Search results for the GEO ID: GSE36530 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM896200 | GPL1261 |
|
WT_STI_0Gy_Rep_1
|
Wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from G1-phase pre-B cells
|
Sample_geo_accession | GSM896200
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896200/suppl/GSM896200_11010_WT_STI_0Gy_Rep_1_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896200/suppl/GSM896200_11010_WT_STI_0Gy_Rep_1_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
|
GSM896201 | GPL1261 |
|
WT_STI_1Gy_Rep_1
|
Irradiated wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from irradiated G1-phase pre-B cells
|
Sample_geo_accession | GSM896201
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896201/suppl/GSM896201_11011_WT_STI_1Gy_Rep_1_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896201/suppl/GSM896201_11011_WT_STI_1Gy_Rep_1_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
|
GSM896202 | GPL1261 |
|
WT_STI_0Gy_Rep_2
|
Wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from G1-phase pre-B cells
|
Sample_geo_accession | GSM896202
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896202/suppl/GSM896202_11014_WT_STI_0Gy_Rep_2_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896202/suppl/GSM896202_11014_WT_STI_0Gy_Rep_2_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
|
GSM896203 | GPL1261 |
|
WT_STI_1Gy_Rep_2
|
Irradiated wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from irradiated G1-phase pre-B cells
|
Sample_geo_accession | GSM896203
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896203/suppl/GSM896203_11015_WT_STI_1Gy_Rep_2_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896203/suppl/GSM896203_11015_WT_STI_1Gy_Rep_2_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
|
GSM896204 | GPL1261 |
|
WT_STI_0Gy_Rep_3
|
Wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from G1-phase pre-B cells
|
Sample_geo_accession | GSM896204
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896204/suppl/GSM896204_11018_WT_STI_0Gy_Rep_3_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896204/suppl/GSM896204_11018_WT_STI_0Gy_Rep_3_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
|
GSM896205 | GPL1261 |
|
WT_STI_1Gy_Rep_3
|
Irradiated wild type v-abl-transformed pre-B cell
|
cell type: G1-phase pre-B cell line
genotype/variation: v-abl-transformed
|
Gene expression from irradiated G1-phase pre-B cells
|
Sample_geo_accession | GSM896205
| Sample_status | Public on Mar 13 2013
| Sample_submission_date | Mar 15 2012
| Sample_last_update_date | Mar 13 2013
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Cells treated with STI571 were passaged with 3 μM STI-571 (Imatinib Mesylate) added to the media and incubated for 48 hr. Cells were irradiated at a rate of 0.72 Gy/min for a final dose of 1 Gy in a Cesium source irradiator and pelleted 2 hr following irradiation.
| Sample_growth_protocol_ch1 | Cells were maintained in suspension in Dulbecco's modified Eagle Medium (DMEM), high glucose, (Gibco BRL 11960-077) supplemented with 10% fetal bovine serum, 1X Sodium Pyruvate (Gibco BRL 11360-070), 1X Non-Essential Amino Acids (Gibco BRL 11140-050), 1X L-Glutamine (Gibco BRL 25030-081), and 2 μl of beta-mercaptoethanol.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was isolated using Qiagen RNeasy technology following the manufacturer’s instructions, including the addition of DNase.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | One microgram of total RNA was amplified as directed in the Affymetrix 3’ IVT Express kit protocol, performing the IVT reaction for 16 hours. Twelve and a half micrograms of amplified biotin-aRNAs were fragmented.
| Sample_hyb_protocol | Ten micrograms of fragmented RNA were hybridized to each array for 16 hours at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol.
| Sample_scan_protocol | Arrays were scanned in an Affymetrix Scanner 3000.
| Sample_data_processing | Data was obtained using the GeneChip® Command Console Software (AGCC; Version 1.1) and using the MAS5 algorithm to generate .CHP files.
| Sample_platform_id | GPL1261
| Sample_contact_name | NIEHS,,Microarray Core
| Sample_contact_email | microarray@niehs.nih.gov, liuliw@niehs.nih.gov
| Sample_contact_laboratory | Microarray Core
| Sample_contact_department | DIR
| Sample_contact_institute | NIEHS
| Sample_contact_address | 111 T.W. Alexander Drive
| Sample_contact_city | RTP
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 27709
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896205/suppl/GSM896205_11019_WT_STI_1Gy_Rep_3_Mouse430_2_.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM896nnn/GSM896205/suppl/GSM896205_11019_WT_STI_1Gy_Rep_3_Mouse430_2_.mas5.CHP.gz
| Sample_series_id | GSE36530
| Sample_data_row_count | 45101
| |
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