Result

Search results for the GEO ID: GSE19601

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM488994

GPL1261

CD4T_WT_TGF(-)

Murine purified wild-type CD4+ T cells stimulated without TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: wild-type treatment group: without TGF-b for 24hr

Gene expression data from wild-type CD4+ T cells cultured without TGF-b for 24hr.

Sample_geo_accession	GSM488994
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488994/suppl/GSM488994.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488994/suppl/GSM488994.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM488995

GPL1261

CD4T_WT_TGF(+)

Murine purified wild-type CD4+ T cells stimulated with TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: wild-type treatment group: with TGF-b for 24hr

Gene expression data from wild-type CD4+ T cells cultured with TGF-b for 24hr.

Sample_geo_accession	GSM488995
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488995/suppl/GSM488995.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488995/suppl/GSM488995.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM488996

GPL1261

CD4T_S2_TGF(-)

Murine purified Smad2-deficient CD4+ T cells stimulated without TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad2del/del treatment group: without TGF-b for 24hr

Gene expression data from Smad2-deficient CD4+ T cells cultured without TGF-b for 24hr.

Sample_geo_accession	GSM488996
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488996/suppl/GSM488996.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488996/suppl/GSM488996.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM488997

GPL1261

CD4T_S2_TGF(+)

Murine purified Smad2-deficient CD4+ T cells stimulated with TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad2del/del treatment group: with TGF-b for 24hr

Gene expression data from Smad2-deficient CD4+ T cells cultured with TGF-b for 24hr.

Sample_geo_accession	GSM488997
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488997/suppl/GSM488997.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488997/suppl/GSM488997.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM488998

GPL1261

CD4T_S3_TGF(-)

Murine purified Smad3-deficient CD4+ T cells stimulated without TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad3-/- treatment group: without TGF-b for 24hr

Gene expression data from Smad3-deficient CD4+ T cells cultured without TGF-b for 24hr.

Sample_geo_accession	GSM488998
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488998/suppl/GSM488998.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488998/suppl/GSM488998.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM488999

GPL1261

CD4T_S3_TGF(+)

Murine purified Smad3-deficient CD4+ T cells stimulated with TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad3-/- treatment group: with TGF-b for 24hr

Gene expression data from Smad3-deficient CD4+ T cells cultured with TGF-b for 24hr.

Sample_geo_accession	GSM488999
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488999/suppl/GSM488999.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM488nnn/GSM488999/suppl/GSM488999.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM489000

GPL1261

CD4T_S23h_TGF(-)

Murine purified Smad2-deficient/Smad3-hetero CD4+ T cells stimulated without TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad2del/del, Smad3+/- treatment group: without TGF-b for 24hr

Gene expression data from Smad2-deficient/Smad3-hetero CD4+ T cells cultured without TGF-b for 24hr.

Sample_geo_accession	GSM489000
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489000/suppl/GSM489000.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489000/suppl/GSM489000.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

GSM489001

GPL1261

CD4T_S23h_TGF(+)

Murine purified Smad2-deficient/Smad3-hetero CD4+ T cells stimulated with TGF-b for 24hr

strain: C57BL/6J cell type: CD4+ T cells genome/variation: Smad2del/del, Smad3+/- treatment group: with TGF-b for 24hr

Gene expression data from Smad2-deficient/Smad3-hetero CD4+ T cells cultured with TGF-b for 24hr.

Sample_geo_accession	GSM489001
Sample_status	Public on Jun 22 2010
Sample_submission_date	Dec 22 2009
Sample_last_update_date	Jun 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	FACS-sorted CD4+CD25-CD44loCD62Lhi T cells (3 x 10^6 cells) were stimulated with plate-bound anti-CD3e (1ug/ml), soluble anti-CD28 (1ug/ml), anti-IFN-g (10ug/ml), anti-IL-4 (10ug/ml) and recombinant murine IL-2 (10ng/ml) in the absence or presence of 2ng/ml of TGF-b for 24 hr.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Trizol extraction of total RNA was performed according to the manufacturer's instructions. As a last step of the extraction procedure, the RNA was purified with the RNeasy Mini-kit (Qiagen, Hilden, Germany).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
Sample_hyb_protocol	Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Sample_scan_protocol	GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Sample_data_processing	The data were analyzed with GeneChip Operating Software 1.4 (GCOS 1.4) using Affymetrix default analysis settings and global scaling as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Tomohito,,Takimoto
Sample_contact_email	takimoto@bioreg.kyushu-u.ac.jp
Sample_contact_phone	+81-3-5363-3483
Sample_contact_fax	+81-3-5360-1508
Sample_contact_department	Microbiology and Immunology
Sample_contact_institute	Keio University School of Medicine
Sample_contact_address	35 Shinanomachi
Sample_contact_city	Shinjyuku-ku
Sample_contact_state	Tokyo
Sample_contact_zip/postal_code	160-8582
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489001/suppl/GSM489001.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM489nnn/GSM489001/suppl/GSM489001.CHP.gz
Sample_series_id	GSE19601
Sample_data_row_count	45101

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