Search results for the GEO ID: GSE24553  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM605346 | GPL570 |
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Human_PT0808_PT
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Human_thyrocytes_0808_PT
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tissue: thyroid
cell type: primary thyrocytes
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01_08P_No_971
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| Sample_geo_accession | GSM605346
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605346/suppl/GSM605346.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
| | |
|
GSM605347 | GPL570 |
|
Human_PT0808_SAGM
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Human_thyrocytes_0808_SAGM
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tissue: thyroid
cell type: primary thyrocytes
|
02_08S_No_971
|
| Sample_geo_accession | GSM605347
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605347/suppl/GSM605347.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
| | |
|
GSM605348 | GPL570 |
|
Human_PT0811_PT
|
Human_thyrocytes_0811_PT
|
tissue: thyroid
cell type: primary thyrocytes
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03_11P_No_971
|
| Sample_geo_accession | GSM605348
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605348/suppl/GSM605348.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
| | |
|
GSM605349 | GPL570 |
|
Human_PT0811_SAGM
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Human_thyrocytes_0811_SAGM
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tissue: thyroid
cell type: primary thyrocytes
|
04_11S_No_971
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| Sample_geo_accession | GSM605349
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605349/suppl/GSM605349.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
| | |
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GSM605350 | GPL570 |
|
Human_PT0812_PT
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Human_thyrocytes_0812_PT
|
tissue: thyroid
cell type: primary thyrocytes
|
05_12P_No_971
|
| Sample_geo_accession | GSM605350
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605350/suppl/GSM605350.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
| | |
|
GSM605351 | GPL570 |
|
Human_PT0812_SAGM
|
Human_thyrocytes_0812_SAGM
|
tissue: thyroid
cell type: primary thyrocytes
|
06_12S_No_971
|
| Sample_geo_accession | GSM605351
| | Sample_status | Public on Apr 15 2011
| | Sample_submission_date | Oct 06 2010
| | Sample_last_update_date | Apr 15 2011
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | PT: primary thyrocytes were plated with DMEM:F12 (1:2) with 3.3% FBS; SAGM: medium was then replaced with SAGM and incubated for about 2 weeks.
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNAs were extracted with ISOGEN reagent using standard procedure.
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated aRNAs were prepared using Affymetrix recommended protocol. Briefly, cDNA was generated from total RNA (100 ug) and labeled aRNA was transcribed by in vitro transcription.
| | Sample_hyb_protocol | 12.5 ug of aRNAs were hybridized for 16 hr. GeneChips were then washed and stained in the Affymetrix Fluidics Station 450.
| | Sample_scan_protocol | GeneChips were scanned using a GeneChip Scanner 3000.
| | Sample_data_processing | The data was analyzed using Affymetrix GeneChip Command Console and Affymetrix Expression Console.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Norisato,,Mitsutake
| | Sample_contact_email | mitsu@nagasaki-u.ac.jp
| | Sample_contact_phone | +81-95-819-7116
| | Sample_contact_fax | +81-95-819-7117
| | Sample_contact_institute | Nagasaki University
| | Sample_contact_address | 1-12-4 Sakamoto
| | Sample_contact_city | Nagasaki
| | Sample_contact_zip/postal_code | 852-8523
| | Sample_contact_country | Japan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM605nnn/GSM605351/suppl/GSM605351.CEL.gz
| | Sample_series_id | GSE24553
| | Sample_data_row_count | 54675
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