Result

Search results for the GEO ID: GSE7491

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM181524

GPL1355

postnatal day 2, biological repl1 (litter 1)

Lung fibroblasts isolated on postnatal day 2, biological repl1 (litter 1)

Sprague Dawley pooled cells from 5 pups (2-day old) from litter 1

pooled cells from 5 pups (2-day old, before septation) from litter 1

Sample_geo_accession	GSM181524
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181524/suppl/GSM181524.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181525

GPL1355

postnatal day 2, biological repl2 (litter 2)

Lung fibroblasts isolated on postnatal day 2, biological repl2 (litter 2)

Sprague Dawley pooled cells from 5 pups (2-day old) from litter 2

pooled cells from 5 pups (2-day old, before septation) from litter 2

Sample_geo_accession	GSM181525
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181525/suppl/GSM181525.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181526

GPL1355

postnatal day 2, biological repl3 (litter 3)

Lung fibroblasts isolated on postnatal day 2, biological repl3 (litter 3)

Sprague Dawley pooled cells from 5 pups (2-day old) from litter 3

pooled cells from 5 pups (2-day old, before septation) from litter 3

Sample_geo_accession	GSM181526
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181526/suppl/GSM181526.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181527

GPL1355

postnatal day 7, biological repl1 (litter 1)

Lung fibroblasts isolated on postnatal day 7, biological repl1 (litter 1)

Sprague Dawley pooled cells from 4 pups (7-day old) from litter 1

pooled cells from 4 pups (7-day old, progressing secondary septation) from litter 1

Sample_geo_accession	GSM181527
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181527/suppl/GSM181527.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181528

GPL1355

postnatal day 7, biological repl2 (litter 2)

Lung fibroblasts isolated on postnatal day 7, biological repl2 (litter 2)

Sprague Dawley pooled cells from 4 pups (7-day old) from litter 2

pooled cells from 4 pups (7-day old, progressing secondary septation) from litter 2

Sample_geo_accession	GSM181528
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181528/suppl/GSM181528.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181529

GPL1355

postnatal day 7, biological repl3 (litter 3)

Lung fibroblasts isolated on postnatal day 7, biological repl3 (litter 3)

Sprague Dawley pooled cells from 4 pups (7-day old) from litter 3

pooled cells from 4 pups (7-day old, progressing secondary septation) from litter 3

Sample_geo_accession	GSM181529
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181529/suppl/GSM181529.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181530

GPL1355

postnatal day 21, biological repl1 (litter 1)

Lung fibroblasts isolated on postnatal day 21, biological repl1 (litter 1)

Sprague Dawley pooled cells from 4 pups (21-day old) from litter 1

pooled cells from 4 pups (21-day old, terminated secondary septation) from litter 1

Sample_geo_accession	GSM181530
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181530/suppl/GSM181530.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181531

GPL1355

postnatal day 21, biological repl2 (litter 2)

Lung fibroblasts isolated on postnatal day 21, biological repl2 (litter 2)

Sprague Dawley pooled cells from 4 pups (21-day old) from litter 2

pooled cells from 4 pups (21-day old, terminated secondary septation) from litter 2

Sample_geo_accession	GSM181531
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181531/suppl/GSM181531.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

GSM181532

GPL1355

postnatal day 21, biological repl3 (litter 3)

Lung fibroblasts isolated on postnatal day 21, biological repl3 (litter 3)

Sprague Dawley pooled cells from 4 pups (21-day old) from litter 3

pooled cells from 4 pups (21-day old, terminated secondary septation) from litter 3

Sample_geo_accession	GSM181532
Sample_status	Public on Apr 12 2007
Sample_submission_date	Apr 10 2007
Sample_last_update_date	Apr 11 2007
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	Lung cells were dispersed by trypsin and collagenase, then plated onto plastic Petri dishes in MEM-10% FBS and allowed to adhere for 45 min. Non-adherent cells were discarded, and the adherent fibroblasts were rinsed and immediately scrapped and pelleted. Freshly isolated cells were stored at -80°C until RNA extraction.
Sample_growth_protocol_ch1	Rat lung fibroblasts were extemporaneously isolated on postnatal days 2 (saccular stage), 7 (alveolar stage, progressing secondary septation) and 21 (alveolar stage, terminated secondary septation)
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNAs were prepared according to the standard Affymetrix protocol from 10 µg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 10 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneArray Scanner 3000
Sample_data_processing	The data were obtained by processing raw CEL files through the Affy package. Background correction method RMA, normalization method qspline, probe-level correction Pmonly, and summarization method Li-Wong model were used.
Sample_platform_id	GPL1355
Sample_contact_name	Jacques,,Bourbon
Sample_contact_email	jacques.bourbon@creteil.inserm.fr
Sample_contact_phone	00 33 1 49 81 37 33
Sample_contact_fax	00 33 1 49 98 37 33
Sample_contact_department	Faculté de Médecine
Sample_contact_institute	Université de Paris 12
Sample_contact_address	8 rue du Général Sarrail
Sample_contact_city	Créteil
Sample_contact_zip/postal_code	94000
Sample_contact_country	France
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM181nnn/GSM181532/suppl/GSM181532.CEL.gz
Sample_series_id	GSE7491
Sample_data_row_count	31099

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