Result

Search results for the GEO ID: GSE34206

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM844234

GPL1261

Tumor Macrophage Untreated d1 rep1

Tumor macrophage

cell type: tumor macrophage treatment: untreated time: day 1 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844234
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844234/suppl/GSM844234_422MG_1_004A-11H1_D1NT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844234/suppl/GSM844234_422MG_1_004A-11H1_D1NT_UNS.CHP.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844235

GPL1261

Tumor Macrophage Untreated d1 rep2

Tumor macrophage

cell type: tumor macrophage treatment: untreated time: day 1 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844235
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844235/suppl/GSM844235_437MG_1_003A-11H1_D1NT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844235/suppl/GSM844235_437MG_1_003A-11H1_D1NT.mas5.GS.chp.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844236

GPL1261

Tumor Macrophage Untreated d7 rep1

Tumor macrophage

cell type: tumor macrophage treatment: untreated time: day 7 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844236
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844236/suppl/GSM844236_422MG_1_001A-11H1_D7NT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844236/suppl/GSM844236_422MG_1_001A-11H1_D7NT_UNS.CHP.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844237

GPL1261

Tumor Macrophage Untreated d7 rep2

Tumor macrophage

cell type: tumor macrophage treatment: untreated time: day 7 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844237
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844237/suppl/GSM844237_437MG_1_001A-11H1_D7NT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844237/suppl/GSM844237_437MG_1_001A-11H1_D7NT.mas5.GS.chp.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844238

GPL1261

Tumor Macrophage Irradiated d1 rep1

Tumor macrophage

cell type: tumor macrophage treatment: irradiated time: day 1 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844238
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844238/suppl/GSM844238_422MG_1_002A-11H1_D1RT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844238/suppl/GSM844238_422MG_1_002A-11H1_D1RT_UNS.CHP.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844239

GPL1261

Tumor Macrophage Irradiated d1 rep2

Tumor macrophage

cell type: tumor macrophage treatment: irradiated time: day 1 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844239
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844239/suppl/GSM844239_437MG_1_002A-11H1_D1RT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844239/suppl/GSM844239_437MG_1_002A-11H1_D1RT.mas5.GS.chp.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844240

GPL1261

Tumor Macrophage Irradiated d7 rep1

Tumor macrophage

cell type: tumor macrophage treatment: irradiated time: day 7 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844240
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844240/suppl/GSM844240_422MG_1_003A-11H1_D7RT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844240/suppl/GSM844240_422MG_1_003A-11H1_D7RT_UNS.CHP.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

GSM844241

GPL1261

Tumor Macrophage Irradiated d7 rep2

Tumor macrophage

cell type: tumor macrophage treatment: irradiated time: day 7 tumor source: Panc02 cell line genetic background: C57BL/6

Sample_geo_accession	GSM844241
Sample_status	Public on Dec 07 2011
Sample_submission_date	Dec 06 2011
Sample_last_update_date	Dec 15 2011
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	Three daily 20Gy treatment fractions were given using an Elekta Synergy linear accelerator (Atlanta, GA) with 6MV photons incorporating a half beam block to minimize dose to the torso
Sample_growth_protocol_ch1	Tumors were innoculated s.c. in the right leg below the knee at a dose of 2x105 Panc02 cells and allowed to establish for 14-17 days before initiation of treatment. At harvest, the tumor was dissected into approximately 2mm fragments followed by agitation in 1mg/mL collagenase (Invitrogen), 100µg/mL hyaluronidase (Sigma), and 20mg/mL DNase (Sigma) in PBS for 1hr at room temperature. The digest was filtered through 100µm nylon mesh to remove macroscopic debris. Cell suspensions were stained with antibodies specific for CD11b, IA (MHC class II) and Gr1 and CD11b+ IA+ cells were FACS sorted using a BD FACSAria Cell Sorter to greater than 98% purity.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared from FACS sorted CD11b+IA+ cells using a PrepEase RNA Spin Kit (Affymetrix, Cleveland, OH).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	NuGEN Nano Ovation v.2 w/ Encore protocol
Sample_hyb_protocol	Mouse Genome 430 2.0 GeneChip array (3’IVT array assay)
Sample_scan_protocol	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_data_processing	Image processing and expression analysis were performed using Affymetrix GeneChip Command Console (AGCC) v. 2.0.0.1029 and Affymetrix Expression Console v. 1.1 software, respectively.
Sample_platform_id	GPL1261
Sample_contact_name	Michael,,Gough
Sample_contact_department	Earle A Chiles Research Institute
Sample_contact_institute	Providence Cancer Center
Sample_contact_address	4805 NE Glisan St
Sample_contact_city	Portland
Sample_contact_state	OR
Sample_contact_zip/postal_code	97213
Sample_contact_country	USA
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844241/suppl/GSM844241_437MG_1_004A-11H1_D7RT.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM844nnn/GSM844241/suppl/GSM844241_437MG_1_004A-11H1_D7RT.mas5.GS.chp.gz
Sample_series_id	GSE34206
Sample_data_row_count	45101

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