Result

Search results for the GEO ID: GSE18486

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM460255

GPL570

A2780 untreated, rep1

A2780, untreated

cell line: A2780 cell type: adenocarcinoma ovary treatment: Untreated

Gene expression data from A2780 untreated.

Sample_geo_accession	GSM460255
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460255/suppl/GSM460255.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460256

GPL570

A2780 untreated, rep2

A2780, untreated

cell line: A2780 cell type: adenocarcinoma ovary treatment: Untreated

Gene expression data from A2780 untreated.

Sample_geo_accession	GSM460256
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460256/suppl/GSM460256.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460257

GPL570

A2780 untreated, rep3

A2780, untreated

cell line: A2780 cell type: adenocarcinoma ovary treatment: Untreated

Gene expression data from A2780 untreated.

Sample_geo_accession	GSM460257
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460257/suppl/GSM460257.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460258

GPL570

A2780 treated with CDk-125, rep1

A2780, CDk-125

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-125

Gene expression data from A2780 treated with CDK-125.

Sample_geo_accession	GSM460258
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460258/suppl/GSM460258.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460259

GPL570

A2780 treated with CDk-125, rep2

A2780, CDk-125

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-125

Gene expression data from A2780 treated with CDK-125.

Sample_geo_accession	GSM460259
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460259/suppl/GSM460259.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460260

GPL570

A2780 treated with CDk-125, rep3

A2780, CDk-125

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-125

Gene expression data from A2780 treated with CDK-125.

Sample_geo_accession	GSM460260
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460260/suppl/GSM460260.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460261

GPL570

A2780 treated with CDk-509, rep1

A2780, CDk-509

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-509

Gene expression data from A2780 treated with CDK-509.

Sample_geo_accession	GSM460261
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460261/suppl/GSM460261.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460262

GPL570

A2780 treated with CDk-509, rep2

A2780, CDk-509

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-509

Gene expression data from A2780 treated with CDK-509.

Sample_geo_accession	GSM460262
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460262/suppl/GSM460262.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

GSM460263

GPL570

A2780 treated with CDk-509, rep3

A2780, CDk-509

cell line: A2780 cell type: adenocarcinoma ovary treatment: CDk-509

Gene expression data from A2780 treated with CDK-509.

Sample_geo_accession	GSM460263
Sample_status	Public on Jul 14 2010
Sample_submission_date	Oct 08 2009
Sample_last_update_date	Jul 09 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Homo sapiens
Sample_taxid_ch1	9606
Sample_treatment_protocol_ch1	24 hours after seeding, cells were treated with different compounds at a dose equal to 5 time the IC50 for 6 hours and collected using Qiagen lysis buffer RLT (Qiagen cat no. 79216).
Sample_growth_protocol_ch1	A2780 (human adenocarcinoma ovary) from ECACC were seeded in T-75 tissue culture flasks (Corning), 25.000 cells/cm2 in RPMI 1640 (Gibco), pH 7.4, 10% FBS (EUROCLONE Australia-USDA approved, cat. ECSO170D, lot.EUS003383), 2mM L-Glutamine (Gibco), 1x Penicillin-Streptomycin (Gibco) and maintained in 5% CO2 at 37°C with 96% relative humidity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted using Qiagen Rneasy kit (Qiagen cat. no. 74104), starting from total cell lysates.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotin-labeled, fragmented cRNA probes were prepared starting from 1.5 µg of total RNA per replicate sample, using the ‘One-Cycle Target Labeling and Control Reagents’ (Affymetrix, Santa Clara, CA) according to the protocols included in the Affymetrix GeneChip Expression Analysis Technical Manual (www.affymetrix.com).
Sample_hyb_protocol	Samples were hybridized onto Affymetrix GeneChip® Human Genome U133 Plus 2.0 Arrays and processed as manufacturer’s instructions using ‘GeneChip® Hybridization, Wash, and Stain Kit’ components (Affymetrix, Santa Clara, CA).
Sample_scan_protocol	GeneChips were scanned using the GeneChip® Scanner 3000.
Sample_data_processing	Scanned images were first inspected for quality control (QC) using a variety of built-in QC tools from the Bioconductor package [www.bioconductor.org] of R, the open source environment for statistical analysis. Feature intensity values from scanned arrays were normalised and reduced to expression summaries using MAS5 implemented in the R statistical environment.
Sample_platform_id	GPL570
Sample_contact_name	Roberta,,Bosotti
Sample_contact_email	roberta.bosotti@nervianoms.com
Sample_contact_laboratory	Genomics
Sample_contact_department	Biotechnology
Sample_contact_institute	Nerviano Medical Sciences srl
Sample_contact_address	viale Pasteur,10
Sample_contact_city	Nerviano
Sample_contact_state	MI
Sample_contact_zip/postal_code	20014
Sample_contact_country	Italy
Sample_contact_web_link	http://www.nervianoms.com/cont/en/
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM460nnn/GSM460263/suppl/GSM460263.CEL.gz
Sample_series_id	GSE18486
Sample_series_id	GSE18552
Sample_data_row_count	54675

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Transcripts profile based on;

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