Result

Search results for the GEO ID: GSE36414

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM892935

GPL1261

EL08-1D2 rep1

EL08-1D2 mono-culture

cell line: EL08-1D2 cell type: stromal cells culture condition: mono-cultured (control)

Gene expression data of EL08-1D2 cell line

Sample_geo_accession	GSM892935
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892935/suppl/GSM892935_A0.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892935/suppl/GSM892935_A0.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892936

GPL1261

EL08-1D2 rep2

EL08-1D2 mono-culture

cell line: EL08-1D2 cell type: stromal cells culture condition: mono-cultured (control)

Gene expression data of EL08-1D2 cell line

Sample_geo_accession	GSM892936
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892936/suppl/GSM892936_E0.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892936/suppl/GSM892936_E0.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892937

GPL1261

EL08/V128

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V128)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V128 for 5 days

Sample_geo_accession	GSM892937
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892937/suppl/GSM892937_A1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892937/suppl/GSM892937_A1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892938

GPL1261

EL08/V131

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V131)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V131 for 5 days

Sample_geo_accession	GSM892938
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892938/suppl/GSM892938_B1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892938/suppl/GSM892938_B1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892939

GPL1261

EL08/V190

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V190)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V190 for 5 days

Sample_geo_accession	GSM892939
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892939/suppl/GSM892939_C1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892939/suppl/GSM892939_C1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892940

GPL1261

EL08/V172

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V172)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V172 for 5 days

Sample_geo_accession	GSM892940
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892940/suppl/GSM892940_D1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892940/suppl/GSM892940_D1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892941

GPL1261

EL08/V163

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V163)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V163 for 5 days

Sample_geo_accession	GSM892941
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892941/suppl/GSM892941_E1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892941/suppl/GSM892941_E1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

GSM892942

GPL1261

EL08/V211

EL08-1D2 co-cultured with CLL

cell line: EL08-1D2 cell type: stromal cells culture condition: co-cultured for 5 days with leukemic B-cells (CLL V211)

Gene expression data of EL08-1D2 cell line co-cultured with CLL V211 for 5 days

Sample_geo_accession	GSM892942
Sample_status	Public on Mar 08 2013
Sample_submission_date	Mar 10 2012
Sample_last_update_date	Mar 08 2013
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_treatment_protocol_ch1	After 24hours 30x10x6 primary CLL cells were seeded onto the feeder layer of EL08-1D2 cells. After 5 days, CLL cells were separated from co-cultures with stromal cells by repeated washing steps with PBS. Subsequently, single cell suspensions were treated with magnetic anti-CD19 beads to allow removal of remaining CLL cells. Flow-cytometry analysis indicated that more than 99% CD5+CD19+ cells were successfully isolated from CLL-stroma-co-cultures
Sample_growth_protocol_ch1	10x5 EL08-1D2 cells were plated in coated 6cm dishes.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was extracted from EL08-1D2 cells using the miRNeasy Mini Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instruction.
Sample_label_ch1	Biotin
Sample_label_protocol_ch1	Biotinylated cRNA were prepared according to the Affymetrix ExpressKit protocol starting from 200 ng total RNA.
Sample_hyb_protocol	Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip MG-430_2.0. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 using the Affymetrix Hybridization, Wash and Stain Kit.
Sample_scan_protocol	Arrays were scanned in a GeneChip Scanner 3000 with G7 update
Sample_data_processing	The data were analyzed with MAS5 using Affymetrix default analysis settings and global scaling to a target intensity of 1000 as normalization method.
Sample_platform_id	GPL1261
Sample_contact_name	Ludger,,Klein-Hitpass
Sample_contact_email	ludger.klein-hitpass@uni-essen.de
Sample_contact_phone	+49 201 723 85552
Sample_contact_laboratory	BioChip Lab
Sample_contact_department	Universitaetsklinikum
Sample_contact_institute	Institut fuer Zellbiologie
Sample_contact_address	Virchowstr. 173
Sample_contact_city	Essen
Sample_contact_zip/postal_code	D-45122
Sample_contact_country	Germany
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892942/suppl/GSM892942_G1.CEL.gz
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM892nnn/GSM892942/suppl/GSM892942_G1.CHP.gz
Sample_series_id	GSE36414
Sample_series_id	GSE36416
Sample_data_row_count	45101

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