Search results for the GEO ID: GSE10856  |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM275417 | GPL570 |
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hIgG1-treated MDMs_2 days_rep1
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control hlgG1
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MDMs at day 2, biological rep1
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biotinylated cRNA were prepared according to the standard Affymetrix protocol
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| Sample_geo_accession | GSM275417
| | Sample_status | Public on Mar 18 2008
| | Sample_submission_date | Mar 17 2008
| | Sample_last_update_date | Mar 17 2008
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Freshly isolated monocytes were treated for 2 days in the presence of 10 ng/ml M-CSF
| | Sample_growth_protocol_ch1 | Monocytes were cultured with RPMI 1640 with 10% FCS
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA according to the manufacturer's instructions
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| | Sample_hyb_protocol | Fragmentation, hybridizatio, washing and staining were performed according Affymetrix's instructions
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000
| | Sample_data_processing | Background correlation, normalization and log2 transformation were carried out using RMA method with their default settings within the Bioconductor suite for R software package
| | Sample_platform_id | GPL570
| | Sample_contact_name | Yung-Chi,,Chang
| | Sample_contact_department | Microbiology and Immunology
| | Sample_contact_institute | National Yang-Ming University
| | Sample_contact_address | 155, Sec. 2, Li-Nong St.
| | Sample_contact_city | Taipei
| | Sample_contact_zip/postal_code | 112
| | Sample_contact_country | Taiwan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM275nnn/GSM275417/suppl/GSM275417.CEL.gz
| | Sample_series_id | GSE10856
| | Sample_data_row_count | 54675
| | |
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GSM275418 | GPL570 |
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DcR3-treated MDMs_2 days_rep1
|
DcR3 treatment
|
MDMs at day 2, biological rep1
|
biotinylated cRNA were prepared according to the standard Affymetrix protocol
|
| Sample_geo_accession | GSM275418
| | Sample_status | Public on Mar 18 2008
| | Sample_submission_date | Mar 17 2008
| | Sample_last_update_date | Mar 17 2008
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Freshly isolated monocytes were treated for 2 days in the presence of 10 ng/ml M-CSF
| | Sample_growth_protocol_ch1 | Monocytes were cultured with RPMI 1640 with 10% FCS
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA according to the manufacturer's instructions
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| | Sample_hyb_protocol | Fragmentation, hybridizatio, washing and staining were performed according Affymetrix's instructions
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000
| | Sample_data_processing | Background correlation, normalization and log2 transformation were carried out using RMA method with their default settings within the Bioconductor suite for R software package
| | Sample_platform_id | GPL570
| | Sample_contact_name | Yung-Chi,,Chang
| | Sample_contact_department | Microbiology and Immunology
| | Sample_contact_institute | National Yang-Ming University
| | Sample_contact_address | 155, Sec. 2, Li-Nong St.
| | Sample_contact_city | Taipei
| | Sample_contact_zip/postal_code | 112
| | Sample_contact_country | Taiwan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM275nnn/GSM275418/suppl/GSM275418.CEL.gz
| | Sample_series_id | GSE10856
| | Sample_data_row_count | 54675
| | |
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GSM275419 | GPL570 |
|
hIgG1-treated MDMs_2 days_rep2
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control hlgG1
|
MDMs at day 2, biological rep2
|
biotinylated cRNA were prepared according to the standard Affymetrix protocol
|
| Sample_geo_accession | GSM275419
| | Sample_status | Public on Mar 18 2008
| | Sample_submission_date | Mar 17 2008
| | Sample_last_update_date | Mar 17 2008
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Freshly isolated monocytes were treated for 2 days in the presence of 10 ng/ml M-CSF
| | Sample_growth_protocol_ch1 | Monocytes were cultured with RPMI 1640 with 10% FCS
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA according to the manufacturer's instructions
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| | Sample_hyb_protocol | Fragmentation, hybridizatio, washing and staining were performed according Affymetrix's instructions
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000
| | Sample_data_processing | Background correlation, normalization and log2 transformation were carried out using RMA method with their default settings within the Bioconductor suite for R software package
| | Sample_platform_id | GPL570
| | Sample_contact_name | Yung-Chi,,Chang
| | Sample_contact_department | Microbiology and Immunology
| | Sample_contact_institute | National Yang-Ming University
| | Sample_contact_address | 155, Sec. 2, Li-Nong St.
| | Sample_contact_city | Taipei
| | Sample_contact_zip/postal_code | 112
| | Sample_contact_country | Taiwan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM275nnn/GSM275419/suppl/GSM275419.CEL.gz
| | Sample_series_id | GSE10856
| | Sample_data_row_count | 54675
| | |
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GSM275420 | GPL570 |
|
DcR3-treated MDMs_2 days_rep2
|
DcR3 treatment
|
MDMs at day 2, biological rep2
|
biotinylated cRNA were prepared according to the standard Affymetrix protocol
|
| Sample_geo_accession | GSM275420
| | Sample_status | Public on Mar 18 2008
| | Sample_submission_date | Mar 17 2008
| | Sample_last_update_date | Mar 17 2008
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_treatment_protocol_ch1 | Freshly isolated monocytes were treated for 2 days in the presence of 10 ng/ml M-CSF
| | Sample_growth_protocol_ch1 | Monocytes were cultured with RPMI 1640 with 10% FCS
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Trizol extraction of total RNA according to the manufacturer's instructions
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol
| | Sample_hyb_protocol | Fragmentation, hybridizatio, washing and staining were performed according Affymetrix's instructions
| | Sample_scan_protocol | GeneChips were scanned using the GeneChip Scanner 3000
| | Sample_data_processing | Background correlation, normalization and log2 transformation were carried out using RMA method with their default settings within the Bioconductor suite for R software package
| | Sample_platform_id | GPL570
| | Sample_contact_name | Yung-Chi,,Chang
| | Sample_contact_department | Microbiology and Immunology
| | Sample_contact_institute | National Yang-Ming University
| | Sample_contact_address | 155, Sec. 2, Li-Nong St.
| | Sample_contact_city | Taipei
| | Sample_contact_zip/postal_code | 112
| | Sample_contact_country | Taiwan
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM275nnn/GSM275420/suppl/GSM275420.CEL.gz
| | Sample_series_id | GSE10856
| | Sample_data_row_count | 54675
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