Search results for the GEO ID: GSE8514  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM211446 | GPL570 |
|
Normal Adrenal Gland (AN11)
|
Normal Adrenal Gland
|
Genotype: Homo sapiens
|
Gene expression data from normal adrenal gland
|
| Sample_geo_accession | GSM211446
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211446/suppl/GSM211446.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211446/suppl/GSM211446.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211447 | GPL570 |
|
Normal Adrenal Gland (AN14)
|
Normal Adrenal Gland
|
Genotype: Homo sapiens
|
Gene expression data from normal adrenal gland
|
| Sample_geo_accession | GSM211447
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211447/suppl/GSM211447.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211447/suppl/GSM211447.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211448 | GPL570 |
|
Normal Adrenal Gland (AN15)
|
Normal Adrenal Gland
|
Genotype: Homo sapiens
|
Gene expression data from normal adrenal gland
|
| Sample_geo_accession | GSM211448
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211448/suppl/GSM211448.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211448/suppl/GSM211448.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211449 | GPL570 |
|
Normal Adrenal Gland (AN18)
|
Normal Adrenal Gland
|
Genotype: Homo sapiens
|
Gene expression data from normal adrenal gland
|
| Sample_geo_accession | GSM211449
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211449/suppl/GSM211449.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211449/suppl/GSM211449.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211450 | GPL570 |
|
Normal Adrenal Gland (AN26)
|
Normal Adrenal Gland
|
Genotype: Homo sapiens
|
Gene expression data from normal adrenal gland
|
| Sample_geo_accession | GSM211450
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211450/suppl/GSM211450.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211450/suppl/GSM211450.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211451 | GPL570 |
|
Aldosterone-producing adenoma (APA1)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211451
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211451/suppl/GSM211451.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211451/suppl/GSM211451.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211452 | GPL570 |
|
Aldosterone-producing adenoma (APA11)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211452
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211452/suppl/GSM211452.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211452/suppl/GSM211452.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211453 | GPL570 |
|
Aldosterone-producing adenoma (APA12)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211453
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211453/suppl/GSM211453.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211453/suppl/GSM211453.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211454 | GPL570 |
|
Aldosterone-producing adenoma (APA13)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211454
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211454/suppl/GSM211454.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211454/suppl/GSM211454.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211455 | GPL570 |
|
Aldosterone-producing adenoma (APA15)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211455
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211455/suppl/GSM211455.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211455/suppl/GSM211455.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211456 | GPL570 |
|
Aldosterone-producing adenoma (APA19)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211456
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211456/suppl/GSM211456.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211456/suppl/GSM211456.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211457 | GPL570 |
|
Aldosterone-producing adenoma (APA4)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211457
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211457/suppl/GSM211457.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211457/suppl/GSM211457.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211458 | GPL570 |
|
Aldosterone-producing adenoma (APA5)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211458
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211458/suppl/GSM211458.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211458/suppl/GSM211458.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211459 | GPL570 |
|
Aldosterone-producing adenoma (APA6)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211459
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211459/suppl/GSM211459.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211459/suppl/GSM211459.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
GSM211460 | GPL570 |
|
Aldosterone-producing adenoma (APA7)
|
Aldosterone-producing adenoma
|
Genotype: Homo sapiens
|
Gene expression data from aldosterone-producing adenoma
|
| Sample_geo_accession | GSM211460
| | Sample_status | Public on Jul 18 2007
| | Sample_submission_date | Jul 18 2007
| | Sample_last_update_date | Aug 14 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The tissue was pulverized in liquid nitrogen to a powder. Total RNA was extracted using TRIzol Reagent (Invitrogen, Carlsbad, CA). The purity and integrity of the RNA were assessed by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA) and its quantity was determined by NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE).
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001,
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Affymetrix Human Genome U133 Plus 2.0. GeneChips were washed and stained in the Affymetrix Fluidics
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | The data were analyzed with GeneSpring 7.3 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Ping,,Ye
| | Sample_contact_email | pye@mcg.edu
| | Sample_contact_phone | 706 721 8779
| | Sample_contact_fax | 706 721 8360
| | Sample_contact_laboratory | CA 3093
| | Sample_contact_department | Physiology
| | Sample_contact_institute | Medical College of Georgia
| | Sample_contact_address | 1120 15th Street
| | Sample_contact_city | Augusta
| | Sample_contact_state | GA
| | Sample_contact_zip/postal_code | 30912
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211460/suppl/GSM211460.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM211nnn/GSM211460/suppl/GSM211460.CHP.gz
| | Sample_series_id | GSE8514
| | Sample_data_row_count | 54675
| | |
|
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