Search results for the GEO ID: GSE35330 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM866111 | GPL570 |
|
Four hour sample with agonist anti-CD158d mAb, rep 1
|
four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 4 hr
|
Gene expression data from four hour sample with agonist anti-CD158d mAb, rep 1 of 4.
|
Sample_geo_accession | GSM866111
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866111/suppl/GSM866111.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866111/suppl/GSM866111.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866116 | GPL570 |
|
Four hour sample with agonist anti-CD158d mAb, rep 2
|
four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 4 hr
|
Gene expression data from four hour sample with agonist anti-CD158d mAb, rep 2 of 4.
|
Sample_geo_accession | GSM866116
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866116/suppl/GSM866116.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866116/suppl/GSM866116.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866118 | GPL570 |
|
Four hour sample with agonist anti-CD158d mAb, rep 3
|
four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 4 hr
|
Gene expression data from four hour sample with agonist anti-CD158d mAb, rep 3 of 4.
|
Sample_geo_accession | GSM866118
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866118/suppl/GSM866118.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866118/suppl/GSM866118.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866119 | GPL570 |
|
Four hour sample with agonist anti-CD158d mAb, rep 4
|
four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 4 hr
|
Gene expression data from four hour sample with agonist anti-CD158d mAb, rep 4 of 4.
|
Sample_geo_accession | GSM866119
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866119/suppl/GSM866119.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866119/suppl/GSM866119.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866121 | GPL570 |
|
Four hour sample control (cIg), rep 1
|
four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 4 hr
|
Gene expression data from four hour sample control (cIg), rep 1 of 4.
|
Sample_geo_accession | GSM866121
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866121/suppl/GSM866121.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866121/suppl/GSM866121.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866122 | GPL570 |
|
Four hour sample control (cIg), rep 2
|
four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 4 hr
|
Gene expression data from four hour sample control (cIg), rep 2 of 4.
|
Sample_geo_accession | GSM866122
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866122/suppl/GSM866122.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866122/suppl/GSM866122.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866124 | GPL570 |
|
Four hour sample control (cIg), rep 3
|
four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 4 hr
|
Gene expression data from four hour sample control (cIg), rep 3 of 4.
|
Sample_geo_accession | GSM866124
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866124/suppl/GSM866124.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866124/suppl/GSM866124.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866126 | GPL570 |
|
Four hour sample control (cIg), rep 4
|
four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 4 hr
|
Gene expression data from four hour sample control (cIg), rep 4 of 4.
|
Sample_geo_accession | GSM866126
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866126/suppl/GSM866126.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866126/suppl/GSM866126.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866127 | GPL570 |
|
Sixteen hour sample with agonist anti-CD158d mAb, rep 1
|
sixteen hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 16 hr
|
Gene expression data from sixteen hour sample with agonist anti-CD158d mAb, rep 1 of 4.
|
Sample_geo_accession | GSM866127
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866127/suppl/GSM866127.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866127/suppl/GSM866127.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866129 | GPL570 |
|
Sixteen hour sample with agonist anti-CD158d mAb, rep 2
|
sixteen hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 16 hr
|
Gene expression data from sixteen hour sample with agonist anti-CD158d mAb, rep 2 of 4.
|
Sample_geo_accession | GSM866129
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866129/suppl/GSM866129.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866129/suppl/GSM866129.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866130 | GPL570 |
|
Sixteen hour sample with agonist anti-CD158d mAb, rep 3
|
sixteen hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 16 hr
|
Gene expression data from sixteen hour sample with agonist anti-CD158d mAb, rep 3 of 4.
|
Sample_geo_accession | GSM866130
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866130/suppl/GSM866130.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866130/suppl/GSM866130.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866132 | GPL570 |
|
Sixteen hour sample with agonist anti-CD158d mAb, rep 4
|
sixteen hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 16 hr
|
Gene expression data from sixteen hour sample with agonist anti-CD158d mAb, rep 4 of 4.
|
Sample_geo_accession | GSM866132
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866132/suppl/GSM866132.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866132/suppl/GSM866132.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866133 | GPL570 |
|
Sixteen hour sample control (cIg), rep 1
|
sixteen hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 16 hr
|
Gene expression data from sixteen hour sample control (cIg), rep 1 of 4.
|
Sample_geo_accession | GSM866133
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866133/suppl/GSM866133.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866133/suppl/GSM866133.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866135 | GPL570 |
|
Sixteen hour sample control (cIg), rep 2
|
sixteen hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 16 hr
|
Gene expression data from sixteen hour sample control (cIg), rep 2 of 4.
|
Sample_geo_accession | GSM866135
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866135/suppl/GSM866135.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866135/suppl/GSM866135.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866136 | GPL570 |
|
Sixteen hour sample control (cIg), rep 3
|
sixteen hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 16 hr
|
Gene expression data from sixteen hour sample control (cIg), rep 3 of 4.
|
Sample_geo_accession | GSM866136
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866136/suppl/GSM866136.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866136/suppl/GSM866136.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866138 | GPL570 |
|
Sixteen hour sample control (cIg), rep 4
|
sixteen hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 16 hr
|
Gene expression data from sixteen hour sample control (cIg), rep 4 of 4.
|
Sample_geo_accession | GSM866138
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866138/suppl/GSM866138.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866138/suppl/GSM866138.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866140 | GPL570 |
|
Sixty-four hour sample with agonist anti-CD158d mAb, rep 1
|
sixty-four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 64 hr
|
Gene expression data from sixty-four hour sample with agonist anti-CD158d mAb, rep 1 of 4.
|
Sample_geo_accession | GSM866140
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866140/suppl/GSM866140.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866140/suppl/GSM866140.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866141 | GPL570 |
|
Sixty-four hour sample with agonist anti-CD158d mAb, rep 2
|
sixty-four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 64 hr
|
Gene expression data from sixty-four hour sample with agonist anti-CD158d mAb, rep 2 of 4.
|
Sample_geo_accession | GSM866141
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866141/suppl/GSM866141.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866141/suppl/GSM866141.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866142 | GPL570 |
|
Sixty-four hour sample with agonist anti-CD158d mAb, rep 3
|
sixty-four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 64 hr
|
Gene expression data from sixty-four hour sample with agonist anti-CD158d mAb, rep 3 of 4.
|
Sample_geo_accession | GSM866142
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866142/suppl/GSM866142.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866142/suppl/GSM866142.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866143 | GPL570 |
|
Sixty-four hour sample with agonist anti-CD158d mAb, rep 4
|
sixty-four hour sample with agonist anti-CD158d mAb
|
cell type: primary natural killer (NK) cells
treatment: anti-CD158d mAb
time: 64 hr
|
Gene expression data from sixty-four hour sample with agonist anti-CD158d mAb, rep 4 of 4.
|
Sample_geo_accession | GSM866143
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866143/suppl/GSM866143.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866143/suppl/GSM866143.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866144 | GPL570 |
|
Sixty-four hour sample control (cIg), rep 1
|
sixty-four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 64 hr
|
Gene expression data from sixty-four hour sample control (cIg), rep 1 of 4.
|
Sample_geo_accession | GSM866144
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866144/suppl/GSM866144.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866144/suppl/GSM866144.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866145 | GPL570 |
|
Sixty-four hour sample control (cIg), rep 2
|
sixty-four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 64 hr
|
Gene expression data from sixty-four hour sample control (cIg), rep 2 of 4.
|
Sample_geo_accession | GSM866145
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866145/suppl/GSM866145.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866145/suppl/GSM866145.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
|
GSM866146 | GPL570 |
|
Sixty-four hour sample control (cIg), rep 3
|
sixty-four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 64 hr
|
Gene expression data from sixty-four hour sample control (cIg), rep 3 of 4.
|
Sample_geo_accession | GSM866146
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866146/suppl/GSM866146.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866146/suppl/GSM866146.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
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GSM866147 | GPL570 |
|
Sixty-four hour sample control (cIg), rep 4
|
sixty-four hour sample control (cIg)
|
cell type: primary natural killer (NK) cells
treatment: control
time: 64 hr
|
Gene expression data from sixty-four hour sample control (cIg), rep 4 of 4.
|
Sample_geo_accession | GSM866147
| Sample_status | Public on Dec 03 2012
| Sample_submission_date | Jan 25 2012
| Sample_last_update_date | Dec 03 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | NK cells were stimulated with either cIg or anti-CD158d mAb for 4 h, 16 h or 64 h.
| Sample_growth_protocol_ch1 | Primary, resting NK cells from 4 donors.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was isolated with an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNase-free DNaseI (Amersham) was used to remove remaining DNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | cDNA was synthesized and labeled according to manufacturer instructions for Affymetrix.
| Sample_hyb_protocol | Hybridization and fluidics were performed according to standard Affymetrix protocols (http://www.affymetrix.com).
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneChip Scanner 7GPlus according to standard Affymetrix protocols.
| Sample_data_processing | The data were analyzed with GCOS 1.4 using Affymetrix default analysis. The trimmed mean target intensity of each array was arbitrarily set to 1250.
| Sample_platform_id | GPL570
| Sample_contact_name | Dan,,Sturdevant
| Sample_contact_email | dsturdevant@niaid.nih.gov
| Sample_contact_phone | 4063639248
| Sample_contact_institute | NIH
| Sample_contact_address | -
| Sample_contact_city | Hamilton
| Sample_contact_state | MT
| Sample_contact_zip/postal_code | 59840
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866147/suppl/GSM866147.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM866nnn/GSM866147/suppl/GSM866147.CHP.gz
| Sample_series_id | GSE35330
| Sample_data_row_count | 54675
| |
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