Search results for the GEO ID: GSE19627 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM489337 | GPL570 |
|
monocytes_+LPS_1
|
blood, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h medium, 4h LPS stimulation
|
24h medium, 4h LPS stimulation
|
Sample_geo_accession | GSM489337
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489337/suppl/GSM489337.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489338 | GPL570 |
|
monocytes_+LPS_2
|
blood, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h medium, 4h LPS stimulation
|
24h medium, 4h LPS stimulation
|
Sample_geo_accession | GSM489338
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489338/suppl/GSM489338.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489339 | GPL570 |
|
monocytes_+LPS_3
|
blood, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h medium, 4h LPS stimulation
|
24h medium, 4h LPS stimulation
|
Sample_geo_accession | GSM489339
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489339/suppl/GSM489339.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489343 | GPL570 |
|
monocytes_-LPS_1
|
blood, -LPS
|
cell type: myeloid monocytic cells
protocol: 28h medium
|
28h medium
|
Sample_geo_accession | GSM489343
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489343/suppl/GSM489343.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489344 | GPL570 |
|
monocytes_-LPS_2
|
blood, -LPS
|
cell type: myeloid monocytic cells
protocol: 28h medium
|
28h medium
|
Sample_geo_accession | GSM489344
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489344/suppl/GSM489344.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489345 | GPL570 |
|
monocytes_-LPS_3
|
blood, -LPS
|
cell type: myeloid monocytic cells
protocol: 28h medium
|
28h medium
|
Sample_geo_accession | GSM489345
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM oxidized ubiquinone (Q10), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489345/suppl/GSM489345.CEL.gz
| Sample_series_id | GSE19625
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489352 | GPL570 |
|
monocytes_Q10H2_1
|
blood, +Q10H2, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h Q10H2 preincubation, 4h LPS stimulation
|
24h Q10H2 preincubation, 4h LPS stimulation
|
Sample_geo_accession | GSM489352
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM ubiquinol (Q10H2), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489352/suppl/GSM489352.CEL.gz
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489353 | GPL570 |
|
monocytes_Q10H2_2
|
blood, +Q10H2, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h Q10H2 preincubation, 4h LPS stimulation
|
24h Q10H2 preincubation, 4h LPS stimulation
|
Sample_geo_accession | GSM489353
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM ubiquinol (Q10H2), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489353/suppl/GSM489353.CEL.gz
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
GSM489354 | GPL570 |
|
monocytes_Q10H2_3
|
blood, +Q10H2, +LPS
|
cell type: myeloid monocytic cells
protocol: 24h Q10H2 preincubation, 4h LPS stimulation
|
24h Q10H2 preincubation, 4h LPS stimulation
|
Sample_geo_accession | GSM489354
| Sample_status | Public on Dec 22 2010
| Sample_submission_date | Dec 23 2009
| Sample_last_update_date | Dec 22 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | In 6-well plates, cells were pre-incubated with 10 µM ubiquinol (Q10H2), or the respective vehicle controls (KANEKA Corporation, Japan). After 24 hours, cell culture medium was removed and fresh lipopolysaccharide (LPS, E. coli, O55:B5, Sigma Aldrich, Taufkirchen, Germany) containing medium (1 µg/ ml) was added for 4 hours, except in the negative control wells (-LPS).
| Sample_growth_protocol_ch1 | THP-1 cells were cultivated in RPMI medium 1640 (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS and 1% antibiotics (penicillin/ streptomycin) in a humidified incubator containing 5% CO2 at 37°C. Twenty four hours before pre-incubation, cells were plated at a density of 3 x 106 per well in a 6-well plate.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were collected in Qiazol-lysis buffer (Qiagen, Hilden, Germany) and stored at -80 °C until isolation of total RNA.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA was prepared according to the standard Affymetrix protocol (IVT Labeling Kit, Affymetrix).
| Sample_hyb_protocol | 20 µg of fragmented cRNA was hybridized to a Human Genome U133 Plus 2.0 array for 16 hr at 45 °C at 60 rpm. Arrays were washed on GeneChip® Fluidics station 450 (Affymetrix) and stained with streptavidin-phycoerythrin
| Sample_scan_protocol | Microarrays were scanned with a GeneChip® Scanner 3000 7G (Affymetrix) using GCOS software.
| Sample_data_processing | Expression data was normalized with GC-RMA algorithm.
| Sample_platform_id | GPL570
| Sample_contact_name | Frank,,Döring
| Sample_contact_email | sek@molprev.uni-kiel.de
| Sample_contact_department | Human Nutrition and Food Science
| Sample_contact_institute | Christian-Albrechts-University Kiel
| Sample_contact_address | Heinrich-Hecht-Platz 10
| Sample_contact_city | Kiel
| Sample_contact_zip/postal_code | 24118
| Sample_contact_country | Germany
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489354/suppl/GSM489354.CEL.gz
| Sample_series_id | GSE19627
| Sample_data_row_count | 54675
| |
|
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