Search results for the GEO ID: GSE16364 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM410554 | GPL1261 |
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Mouse_ESC_Pcl2_mismatch_control_sample 2
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Undifferentiated mouse embryonic stem cells
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cell type: R1 mouse embryonic stem cells stably transfected with shRNA mismatch control sequence
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Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410554
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | May 29 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing shRNA mismatch control sequence for comparision with Pcl2 shRNA knockdown cells.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37°C and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410554/suppl/GSM410554.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410554/suppl/GSM410554.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
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GSM410802 | GPL1261 |
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Mouse_ESC_Pcl2_mismatch_control_sample 3
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Undifferentiated mouse embryonic stem cells
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cell type: R1 mouse embryonic stem cells stably transfected with shRNA mismatch control sequence
|
Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410802
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | Jun 01 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing shRNA mismatch control sequence for comparision with Pcl2 shRNA knockdown cells.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37°C and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410802/suppl/GSM410802.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410802/suppl/GSM410802.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
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GSM410803 | GPL1261 |
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Mouse_ESC_Pcl2_shRNA_sample 2
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Undifferentiated mouse embryonic stem cells
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cell type: R1 mouse embryonic stem cells stably transfected with Pcl2 shRNA sequence
|
Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410803
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | Jun 01 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing Pcl2 shRNA.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37°C and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410803/suppl/GSM410803.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410803/suppl/GSM410803.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
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GSM410804 | GPL1261 |
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Mouse_ESC_Pcl2_shRNA_sample 3
|
Undifferentiated mouse embryonic stem cells
|
cell type: R1 mouse embryonic stem cells stably transfected with Pcl2 shRNA sequence
|
Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410804
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | Jun 01 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing Pcl2 shRNA.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37°C and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410804/suppl/GSM410804.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410804/suppl/GSM410804.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
|
GSM410829 | GPL1261 |
|
Mouse_ESC_Pcl2_mismatch_control_sample 1
|
Undifferentiated mouse embryonic stem cells
|
cell type: R1 mouse embryonic stem cells stably transfected with shRNA mismatch control sequence
|
Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410829
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | Jun 01 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing shRNA mismatch control sequence for comparision with Pcl2 shRNA knockdown cells.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37ðC and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410829/suppl/GSM410829.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410829/suppl/GSM410829.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
|
GSM410830 | GPL1261 |
|
Mouse_ESC_Pcl2_shRNA_sample 1
|
Undifferentiated mouse embryonic stem cells
|
cell type: R1 mouse embryonic stem cells stably transfected with Pcl2 shRNA sequence
|
Total RNA was extracted from Pcl2 mismatch controls and one Pcl2 shRNA clone with RNeasy columns (Qiagen). RNA quality was tested using an Agilent Bioanalyzer before performing standard cDNA synthesis (Invitrogen Superscript) and in vitro transcription (IVT) (Enzo IVT kit). 10 ug of RNA was used for IVT and 15 ug of cRNA was used for hybridization (EukGEWS2v4 kit) to the Mouse Genome 430 2.0 GeneChip. Scanning was performed using the Affymetrix GeneChip Scanner 3000 and analysis done using GCOS1.4 to obtain signal-log ratios of the control to the sample. Hybridizations of three biological replicates for both the control and Pcl2 shRNA clone were performed.
|
Sample_geo_accession | GSM410830
| Sample_status | Public on Feb 05 2010
| Sample_submission_date | Jun 01 2009
| Sample_last_update_date | Dec 22 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | Stanford Lab, University of Toronto
| Sample_treatment_protocol_ch1 | Cells were stably expressing Pcl2 shRNA.
| Sample_growth_protocol_ch1 | R1 ESCs were cultured at 37°C and 5% CO2, in ESC media consisting of Dulbecco modified eagle serum (DMEM) supplemented with 15% FBS (North Bio, Lot SF30408), 0.1 mM nonessential amino acids, 1 mM sodium pyruvate, 2 mM L-glutamine (all from Gibco), 1000 U/mL leukemia inhibitory factor (LIF) (ESGRO, from Chemicon, batch 11061065) and 100 µM b-mercaptoethanol (Sigma). Differentiation media consisted of either ESC media without LIF, or ESC media without LIF and supplemented with 0.1 uM retinoic acid. Selection media consisted of ESC media supplemented with 150 ug/mL G418 (Gibco). ESCs were passaged every two days at a ratio of 1:5 by washing with PBS (Gibco), dissociating with 0.05% trypsin (Gibco) for 5 minutes at 37ðC and resuspending in ESC media. Media was changed daily.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Qiagen RNeasy column purification
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Enzo IVT kit
| Sample_hyb_protocol | EukGE-WS2v4
| Sample_scan_protocol | Affymetrix GeneChip Scanner 3000
| Sample_data_processing | MAS5
| Sample_platform_id | GPL1261
| Sample_contact_name | William,L,Stanford
| Sample_contact_email | william.stanford@utoronto.ca
| Sample_contact_laboratory | William L. Stanford
| Sample_contact_department | IBBME
| Sample_contact_institute | University of Toronto
| Sample_contact_address | 164 College St
| Sample_contact_city | Toronto
| Sample_contact_state | Ontario
| Sample_contact_zip/postal_code | M5S 3G9
| Sample_contact_country | Canada
| Sample_contact_web_link | http://www.wlstanfordlab.com/
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410830/suppl/GSM410830.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM410nnn/GSM410830/suppl/GSM410830.CHP.gz
| Sample_series_id | GSE16364
| Sample_data_row_count | 45101
| |
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