Search results for the GEO ID: GSE25332  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM623392 | GPL570 |
|
Hec50_mock_rep_1
|
mock
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623392
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623392/suppl/GSM623392.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623393 | GPL570 |
|
Hec50_mock_rep_2
|
mock
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623393
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623393/suppl/GSM623393.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623394 | GPL570 |
|
Hec50_mock_rep_3
|
mock
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623394
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623394/suppl/GSM623394.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623395 | GPL570 |
|
Hec50_neg_rep_1
|
scrambled negative control
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623395
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623395/suppl/GSM623395.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623396 | GPL570 |
|
Hec50_neg_rep_2
|
scrambled negative control
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623396
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623396/suppl/GSM623396.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623397 | GPL570 |
|
Hec50_neg_rep_3
|
scrambled negative control
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623397
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623397/suppl/GSM623397.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623398 | GPL570 |
|
Hec50_200c_rep_1
|
miR-200c mimic
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623398
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623398/suppl/GSM623398.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623399 | GPL570 |
|
Hec50_200c_rep_2
|
miR-200c mimic
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623399
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623399/suppl/GSM623399.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
|
GSM623400 | GPL570 |
|
Hec50_200c_rep_3
|
miR-200c mimic
|
cell line: Hec50
cell type: endometrial cancer
|
Endometrial cancer cell line (Hec50) mock transfected, or transfected with scrambled negative control or miR-200c
|
| Sample_geo_accession | GSM623400
| | Sample_status | Public on Nov 17 2010
| | Sample_submission_date | Nov 15 2010
| | Sample_last_update_date | Nov 17 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Cells were treated with 60 nM miR-200c mimic or scrambled negative control (Applied Biosystems) for 48 hrs prior to extraction
| | Sample_growth_protocol_ch1 | Cells were grown in DMEM supplemented with L-glutamine and 10% FBS in an incubator at 37 degrees and 5% CO2
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to manufacturer's directions. RNA integrity was confirmed using an Agilent Bioanalyzer (Agilent, Palo Alto, CA)
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Labeled complementary RNA was made using the GeneChip_IVT labeling kit (Affymetrix, Inc., Santa Clara, CA)
| | Sample_hyb_protocol | 20 ug biotin-labeled cDNA was fragmented and hybridized.
| | Sample_scan_protocol | Microarray analysis was performed using Affymetrix gene chips (HuFL-U133 plus2) and scanned using Affymetrix Genechip Scanner 3000
| | Sample_data_processing | All entities: Data normalized to chip. 1_5 fold 200c vs mock and neg: Data was analyzed using Genespring GX 9.0 (Agilent). Data was filtered using a 1.5 fold change cutoff and a p value of 0.05 (ANOVA, with Benjamini Hochberg FDR multiple testing correction).
| | Sample_platform_id | GPL570
| | Sample_contact_name | Erin,N.,Howe
| | Sample_contact_email | erin.howe@ucdenver.edu
| | Sample_contact_laboratory | Richer Lab
| | Sample_contact_department | Pathology
| | Sample_contact_institute | University of Colorado at Denver, Anschutz Medical Campus
| | Sample_contact_address | UCD AMC, Mail Stop 8104 PO Box 6511
| | Sample_contact_city | Aurora
| | Sample_contact_state | CO
| | Sample_contact_zip/postal_code | 80045
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM623nnn/GSM623400/suppl/GSM623400.CEL.gz
| | Sample_series_id | GSE25332
| | Sample_data_row_count | 54675
| | |
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