Search results for the GEO ID: GSE19735  |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM492826 | GPL570 |
|
Day 14 hESC Ebs_1
|
hESC Ebs differentiated for 14 days in pro-angiogenic cytokines
|
developmental stage: embroynic
cell type: Embryonic Stem Cells (hESCs)
|
d14 EB_1
|
| Sample_geo_accession | GSM492826
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492826/suppl/GSM492826.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492826/suppl/GSM492826.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492827 | GPL570 |
|
Day 14 hESC Ebs_2
|
hESC Ebs differentiated for 14 days in pro-angiogenic cytokines
|
developmental stage: embroynic
cell type: Embryonic Stem Cells (hESCs)
|
d14 EB_2
|
| Sample_geo_accession | GSM492827
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492827/suppl/GSM492827.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492827/suppl/GSM492827.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492828 | GPL570 |
|
Day 14 hESC ECs_1
|
purified hESC-derived ECs isolated at day 14 of differentiation in the presence of TGFbeta inhibition
|
developmental stage: embroynic
cell type: hESC-derived Endothelial Cells
genome/variation: EC-specific VE-cadherin promoter driving GFP (hVPr-GFP)
|
Phase 1 VPrGFP_1
|
| Sample_geo_accession | GSM492828
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492828/suppl/GSM492828.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492828/suppl/GSM492828.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492829 | GPL570 |
|
Day 14 hESC ECs_2
|
purified hESC-derived ECs isolated at day 14 of differentiation in the presence of TGFbeta inhibition
|
developmental stage: embroynic
cell type: hESC-derived Endothelial Cells
genome/variation: EC-specific VE-cadherin promoter driving GFP (hVPr-GFP)
|
Phase 1 VPrGFP_2
|
| Sample_geo_accession | GSM492829
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492829/suppl/GSM492829.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492829/suppl/GSM492829.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492830 | GPL570 |
|
Day 24 hESC ECs_1
|
purified hESC-derived ECs isolated at day 14 of differentiation and cultured for an additional 10 days in the presence of TGFbeta inhibition
|
developmental stage: embroynic
cell type: hESC-derived Endothelial Cells
genome/variation: EC-specific VE-cadherin promoter driving GFP (hVPr-GFP)
|
Phase 2 VPrGFP+SB_1
|
| Sample_geo_accession | GSM492830
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492830/suppl/GSM492830.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492830/suppl/GSM492830.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492831 | GPL570 |
|
Day 24 hESC ECs_2
|
purified hESC-derived ECs isolated at day 14 of differentiation and cultured for an additional 10 days in the presence of TGFbeta inhibition
|
developmental stage: embroynic
cell type: hESC-derived Endothelial Cells
genome/variation: EC-specific VE-cadherin promoter driving GFP (hVPr-GFP)
|
Phase 2 VPrGFP+SB_2
|
| Sample_geo_accession | GSM492831
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492831/suppl/GSM492831.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492831/suppl/GSM492831.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492832 | GPL570 |
|
Human Umbilical Vein ECs_1
|
Human Umbilical Vein ECs cultured in serum free conditions for 48 hours
|
developmental stage: mature
cell type: Umbilical Vein Endothelial Cells
|
HUVEC_1
|
| Sample_geo_accession | GSM492832
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492832/suppl/GSM492832.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492832/suppl/GSM492832.CHP.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492833 | GPL570 |
|
Human Umbilical Vein ECs_2
|
Human Umbilical Vein ECs cultured in serum free conditions for 48 hours
|
developmental stage: mature
cell type: Umbilical Vein Endothelial Cells
|
HUVEC_2
|
| Sample_geo_accession | GSM492833
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492833/suppl/GSM492833.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492833/suppl/GSM492833.CHP.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492834 | GPL570 |
|
Human Umbilical Vein Smooth Muscle Cells_1
|
Human Umbilical Vein Smooth Muscle Cells cultured in serum free conditions for 48 hours
|
developmental stage: mature
cell type: Umbilical Vein Endothelial Cells
|
SMC_1
|
| Sample_geo_accession | GSM492834
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492834/suppl/GSM492834.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492834/suppl/GSM492834.CHP.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492835 | GPL570 |
|
Human Umbilical Vein Smooth Muscle Cells_2
|
Human Umbilical Vein Smooth Muscle Cells cultured in serum free conditions for 48 hours
|
developmental stage: mature
cell type: Umbilical Vein Endothelial Cells
|
SMC_2
|
| Sample_geo_accession | GSM492835
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Aug 15 2013
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492835/suppl/GSM492835.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492835/suppl/GSM492835.CHP.gz
| | Sample_relation | Reanalyzed by: GSE49910
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492836 | GPL570 |
|
Human Cord Blood CD34+ Cells_1
|
isolated and Human Cord Blood CD34+ Cells
|
developmental stage: mature
cell type: Cord Blood CD34+ Cells
|
CD34_1
|
| Sample_geo_accession | GSM492836
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492836/suppl/GSM492836.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492836/suppl/GSM492836.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
| | |
|
GSM492837 | GPL570 |
|
Human Cord Blood CD34+ Cells_2
|
isolated and Human Cord Blood CD34+ Cells
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developmental stage: mature
cell type: Cord Blood CD34+ Cells
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CD34_2
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| Sample_geo_accession | GSM492837
| | Sample_status | Public on Jan 05 2010
| | Sample_submission_date | Jan 04 2010
| | Sample_last_update_date | Jan 04 2010
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Homo sapiens
| | Sample_taxid_ch1 | 9606
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | The protocol used to extract RNA was according to Manufacturers specifications QIAGEN RNeasy kit.
| | Sample_label_ch1 | Biotin
| | Sample_label_protocol_ch1 | The Superscript choice kit (Invitrogen, Carlsbad,CA) was used to make cDNA with a T7-(dT)24 primer incorporating a T7 RNA polymerase promoter. The biotin labeled cRNA was made by in vitro transcription (Enzo Diagnostics).
| | Sample_hyb_protocol | Fragmented cRNA was hybridized to the gene chips, washed, and stained with streptavidin phycoerythrin.
| | Sample_scan_protocol | The probe arrays were scanned with the Genechip System confocal scanner.
| | Sample_data_processing = Affymetrix Microarray suite 5.0 was used to analyze the data using default settings. Raw values with standard error between biological duplicates; cutoff | minimal expression 100 in at least one group.
| | Sample_platform_id | GPL570
| | Sample_contact_name | Shahin,,Rafii
| | Sample_contact_email | srafii@med.cornell.edu
| | Sample_contact_phone | 212 746 2017
| | Sample_contact_institute | Weill Cornell Medical College
| | Sample_contact_address | 1300 York Avenue
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10065
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492837/suppl/GSM492837.CEL.gz
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM492nnn/GSM492837/suppl/GSM492837.CHP.gz
| | Sample_series_id | GSE19735
| | Sample_data_row_count | 54675
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