Search results for the GEO ID: GSE31359 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM777543 | GPL1261 |
|
NC-EpH4
|
Mammary gland epithelial cells (EMT resistance)
|
tissue: Mammary gland
treatment: resting epithelial cells
|
Gene expression data from resting epithelial cells
|
Sample_geo_accession | GSM777543
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777543/suppl/GSM777543_2654-G1-NC-EpH4.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777544 | GPL1261 |
|
EMT-EpH4
|
EMT-induced mammary gland epithelial cells (EMT resistance)
|
tissue: Mammary gland
treatment: epithelial cells stimulated with TGF-b1/EGF
|
Gene expression data from epithelial cells stimulated with TGF-b1/EGF
|
Sample_geo_accession | GSM777544
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777544/suppl/GSM777544_2655-G1-EMT-EpH4.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777545 | GPL1261 |
|
NC-mProx
|
Proximal renal tubular epithelial cells
|
tissue: Kidney
treatment: resting epithelial cells
|
Gene expression data from resting epithelial cells
|
Sample_geo_accession | GSM777545
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777545/suppl/GSM777545_2656-G1-2328NC_mProx.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777546 | GPL1261 |
|
EMT-mProx
|
EMT-induced proximal renal tubular epithelial cells
|
tissue: Kidney
treatment: epithelial cells stimulated with TGF-b1/EGF
|
Gene expression data from epithelial cells stimulated with TGF-b1/EGF
|
Sample_geo_accession | GSM777546
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777546/suppl/GSM777546_2657-G1-2329EMT_mProx.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777547 | GPL1261 |
|
NC-MCT
|
Renal tubular epithelial cells
|
tissue: Kidney
treatment: resting epithelial cells
|
Gene expression data from resting epithelial cells
|
Sample_geo_accession | GSM777547
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777547/suppl/GSM777547_2658-G1-2398NC-MCT.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777548 | GPL1261 |
|
EMT-MCT
|
EMT-induced renal tubular epithelial cells
|
tissue: Kidney
treatment: epithelial cells stimulated with TGF-b1/EGF
|
Gene expression data from epithelial cells stimulated with TGF-b1/EGF
|
Sample_geo_accession | GSM777548
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777548/suppl/GSM777548_2659-G1-2399EMT-MCT.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777549 | GPL1261 |
|
NC-NMuMG
|
Mammary gland epithelial cells
|
tissue: Mammary gland
treatment: resting epithelial cells
|
Gene expression data from resting epithelial cells
|
Sample_geo_accession | GSM777549
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777549/suppl/GSM777549_2660-G1-2400NC-NMuMG.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
GSM777550 | GPL1261 |
|
EMT-NMuMG
|
EMT-induced mammary gland epithelial cells
|
tissue: Mammary gland
treatment: epithelial cells stimulated with TGF-b1/EGF
|
Gene expression data from epithelial cells stimulated with TGF-b1/EGF
|
Sample_geo_accession | GSM777550
| Sample_status | Public on Aug 13 2011
| Sample_submission_date | Aug 12 2011
| Sample_last_update_date | Aug 13 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | Treated with or without rhTGF-b1 3.0 ng/mL and rhEGF 3.0 ng/mL in K-1 medium for 24 hours.
| Sample_growth_protocol_ch1 | Seeded in six-well plates (1x105 cells/well) and incubated overnight in DMEM containing 10% FCS, after which the medium was replaced with modified K-1 medium (50:50 Ham's F-12/DMEM with 5μg/ml transferrin and 5μg/ml insulin), and the cells were incubated for further 24 hours.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was extracted by using RNeasy mini-kit (Qiagen) according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labelled.
| Sample_hyb_protocol | Biotinylated cRNA was hybridized with a probe array for 16h at 45C, and the hybridized biotinylated cRNA was stained with streptavidin-PE.
| Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner (Palo Alto).
| Sample_data_processing | The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100.
| Sample_platform_id | GPL1261
| Sample_contact_name | Akihiro,,Umezawa
| Sample_contact_email | umezawa@1985.jukuin.keio.ac.jp
| Sample_contact_phone | 81-3-5494-7047
| Sample_contact_fax | 81-3-5494-7048
| Sample_contact_department | Reproductive Biology
| Sample_contact_institute | National Center for Child Health and Development
| Sample_contact_address | 2-10-1 Okura
| Sample_contact_city | Setagaya-ku
| Sample_contact_state | Tokyo
| Sample_contact_zip/postal_code | 157-8535
| Sample_contact_country | Japan
| Sample_contact_web_link | http://1985.jukuin.keio.ac.jp/umezawa/HTML
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM777nnn/GSM777550/suppl/GSM777550_2661-G1-2401EMT-NMuMG.CEL.gz
| Sample_series_id | GSE31359
| Sample_data_row_count | 45101
| |
|
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