Result

Search results for the GEO ID: GSE36174

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Title

Source name

Description

Characteristics

GSM882304

GPL85

Rat Lung at Day 0, biological rep1

Rat 8-10 wks exposed to LPS intranasally at Day 0

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 0 post LPS exposure

Sample_geo_accession	GSM882304
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882304/suppl/GSM882304_Control_1_Metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882304/suppl/GSM882304_FG_RatAsthma_Control_1_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882304/suppl/GSM882304_FG_RatAsthma_Control_1_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

GSM882306

GPL85

Rat Lung at Day 0, biological rep2

Rat 8-10 wks exposed to LPS intranasally at Day 0

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 0 post LPS exposure

Sample_geo_accession	GSM882306
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882306/suppl/GSM882306_Control_2_Metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882306/suppl/GSM882306_FG_RatAsthma_Control_2_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882306/suppl/GSM882306_FG_RatAsthma_Control_2_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

GSM882307

GPL85

Rat Lung at Day 0, biological rep3

Rat 8-10 wks exposed to LPS intranasally at Day 0

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 0 post LPS exposure

Sample_geo_accession	GSM882307
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882307/suppl/GSM882307_Control_3_Metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882307/suppl/GSM882307_FG_RatAsthma_Control_3_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882307/suppl/GSM882307_FG_RatAsthma_Control_3_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

GSM882309

GPL85

Rat Lung at Day 2, biological rep1

Rat 8-10 wks exposed to LPS intranasally at Day 2

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 2 post LPS exposure

Sample_geo_accession	GSM882309
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882309/suppl/GSM882309_2DayAfterLPS_1_metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882309/suppl/GSM882309_FG_RatAsthma_2DayAfterLPS_1_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882309/suppl/GSM882309_FG_RatAsthma_2DayAfterLPS_1_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

GSM882310

GPL85

Rat Lung at Day 2, biological rep2

Rat 8-10 wks exposed to LPS intranasally at Day 2

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 2 post LPS exposure

Sample_geo_accession	GSM882310
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882310/suppl/GSM882310_2DayAfterLPS_2_metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882310/suppl/GSM882310_FG_RatAsthma_2DayAfterLPS_2_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882310/suppl/GSM882310_FG_RatAsthma_2DayAfterLPS_2_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

GSM882312

GPL85

Rat Lung at Day 2, biological rep3

Rat 8-10 wks exposed to LPS intranasally at Day 2

age: 8-10 wks age Sex: Male strain: F344/ NCrR genotype: wild type

Gene expression data from lung epithelial cells at Day 2 post LPS exposure

Sample_geo_accession	GSM882312
Sample_status	Public on Mar 01 2012
Sample_submission_date	Feb 29 2012
Sample_last_update_date	Mar 01 2012
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Rattus norvegicus
Sample_taxid_ch1	10116
Sample_treatment_protocol_ch1	For intratracheal instillations, rats were briefly anesthetized with 5% isoflurane in oxygen and instilled intranasally with 1000 μg of LPS (Pseudomonas aeruginosa serotype 10, lot 31K4122, 3,000,000 LPS units (EU)/mg, Sigma, St. Louis, MO) in 0.5 ml of 0.9% pyrogen-free saline. Control rats were not instilled.
Sample_growth_protocol_ch1	Specific pathogen-free F344/NCrR male rats of 6–8 wk of age were obtained from NCI (Frederick, MD) and were housed until 8–10 weeks of age. The rats were housed in pairs and were provided food and water ad libitum, a 12-h light/dark cycle at 22.2°C, and 30-40% humidity. Rats were weighed and randomly assigned to each experimental group.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	The right lungs of F344/NCrR male rats at 0 and 2 d post LPS instillation were snap-frozen, and stored at -80 C after inflating with diluted (1:4 in PBS) Tissue-Tek O.C.T. (EMS Biosciences, Hatfeild, PA). Frozen tissue sections (8 μm thick) were fixed, dehydrated, air-dried, and epithelial cells from five large airways of each rat were captured using the laser onto Arcturus® CapSure® HS LCM Caps (Applied Biosystems, Foster City, CA). Total RNA was extracted from the cellular lysate in the cap using the PicoPure® RNA Isolation Kit (Applied Biosystems).
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	mRNA were amplified using the RiboAmp RNA amplification kit (Applied Biosystems) as per manufacturer’s instructions. Epithelia microdissected from eight tissue sections resulted in an average 1000 ng of amplified RNA. A second round of amplification was carried out and the biotinylated cRNA probes were then prepared.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA (in 200 ul) were hybridized for 16 hr at 45 C on rat microarray chip RG-U34A (Affymetrix Inc., Sunnyvale, CA). Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400. Microarray Chips were washed and stained in the Affymetrix GeneChip Fluidics Station 400.
Sample_scan_protocol	Microarray Chips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Sample_data_processing	The data were analyzed with Microarray Suite version 4.0 (MAS 4.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1500.
Sample_platform_id	GPL85
Sample_contact_name	Hitendra,,Chand
Sample_contact_email	hchand@lrri.org
Sample_contact_phone	505-348-8774
Sample_contact_institute	Lovelace Respiraotry Research Institute
Sample_contact_address	2425 Ridgecrest Dr SE
Sample_contact_city	Albuquerque
Sample_contact_state	NM
Sample_contact_zip/postal_code	87108
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882312/suppl/GSM882312_2DayAfterLPS_3_metrics.TXT.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882312/suppl/GSM882312_FG_RatAsthma_2DayAfterLPS_3_RGU34A.CEL.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM882nnn/GSM882312/suppl/GSM882312_FG_RatAsthma_2DayAfterLPS_3_RGU34A.CHP.gz
Sample_series_id	GSE36174
Sample_data_row_count	8799

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