Search results for the GEO ID: GSE28093 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM694419 | GPL1261 |
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OPC-CG4_1
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mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
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Sample_geo_accession | GSM694419
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694419/suppl/GSM694419.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
|
GSM694420 | GPL1261 |
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OPC-CG4_2
|
mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
|
|
Sample_geo_accession | GSM694420
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694420/suppl/GSM694420.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
|
GSM694421 | GPL1261 |
|
OPC-FCS_1
|
mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
|
|
Sample_geo_accession | GSM694421
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694421/suppl/GSM694421.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
|
GSM694422 | GPL1261 |
|
OPC-FCS_2
|
mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
|
|
Sample_geo_accession | GSM694422
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694422/suppl/GSM694422.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
|
GSM694423 | GPL1261 |
|
OPC-Rev_1
|
mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
|
|
Sample_geo_accession | GSM694423
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694423/suppl/GSM694423.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
|
GSM694424 | GPL1261 |
|
OPC-Rev_2
|
mouse OPC
|
cell type: oligodendrocyte precursor cells
strain: C57BL6
tissue: brain
age: postnatal day 0
|
|
Sample_geo_accession | GSM694424
| Sample_status | Public on Jun 01 2011
| Sample_submission_date | Mar 22 2011
| Sample_last_update_date | Jun 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Oligodendrocyte precursor cells were prepared from postnatal day 0 mouse brain and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared using a RNeasy Mini Kit (QIAGEN).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
| Sample_hyb_protocol | Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
| Sample_scan_protocol | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
| Sample_data_processing | The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
| Sample_platform_id | GPL1261
| Sample_contact_name | Toru,,Kondo
| Sample_contact_email | tkondo@cdb.riken.jp
| Sample_contact_phone | +81-78-306-3170
| Sample_contact_fax | +81-78-306-3171
| Sample_contact_laboratory | Laboratory for Cell Lineage Modulation
| Sample_contact_department | Center for Developmental Biology
| Sample_contact_institute | RIKEN
| Sample_contact_address | 2-2-3, Minatojima-Minamimachi, Chuo-ku
| Sample_contact_city | Kobe
| Sample_contact_zip/postal_code | 650-0047
| Sample_contact_country | Japan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM694nnn/GSM694424/suppl/GSM694424.CEL.gz
| Sample_series_id | GSE28093
| Sample_data_row_count | 45101
| |
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