Search results for the GEO ID: GSE19672 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM491168 | GPL570 |
|
48h siRNA rep1
|
human corporal smooth muscle cells, MaxiK expression silenced for 48h
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491168
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491168/suppl/GSM491168_KD1-HG-U133_Plus_2-3304.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491169 | GPL570 |
|
48h siRNA rep2
|
human corporal smooth muscle cells, MaxiK expression silenced for 48h
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491169
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491169/suppl/GSM491169_KD1-HG-U133_Plus_2-3305.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491170 | GPL570 |
|
48h siRNA rep3
|
human corporal smooth muscle cells, MaxiK expression silenced for 48h
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491170
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491170/suppl/GSM491170_KD1-HG-U133_Plus_2-3519.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491171 | GPL570 |
|
48h siRNA rep4
|
human corporal smooth muscle cells, MaxiK expression silenced for 48h
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491171
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491171/suppl/GSM491171_KD1-HG-U133_Plus_2-3520.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491172 | GPL570 |
|
untreated rep1
|
human corporal smooth muscle cells, untreated
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491172
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491172/suppl/GSM491172_KD1-HG-U133_Plus_2-3306.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491173 | GPL570 |
|
untreated rep2
|
human corporal smooth muscle cells, untreated
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491173
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491173/suppl/GSM491173_KD1-HG-U133_Plus_2-3307.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
|
GSM491174 | GPL570 |
|
untreated rep3
|
human corporal smooth muscle cells, untreated
|
cell type: corpus cavernosum smooth muscle cell
|
n/a
|
Sample_geo_accession | GSM491174
| Sample_status | Public on Dec 25 2010
| Sample_submission_date | Dec 28 2009
| Sample_last_update_date | Dec 25 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | Silencing of MaxiK expression was obtained using Stealth Select RNAi (Invitrogen). Cultured cells were transfected with 30nM siRNA using Lipofectamine RNAiMAX transfection reagent (Invitrogen) following the instructions of the manufacturer.
| Sample_growth_protocol_ch1 | Penile tissue was obtained from patients undergoing surgery for implantation of prostheses. Explant cell cultures were grown in DMEM, 10% fetal bovine serum (Invitrogen)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Cells were harvested 48h after transfection and RNA was isolated using RNeasy Mini Kit (Quiagen). Efficacy of silencing (>90%) was confirmed by quantitative RT-PCR.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_hyb_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_scan_protocol | Labeling, hybridization and scanning were performed by the Affymetrix facility at Albert Einstein College of Medicine following standard Affymetrix protocols
| Sample_data_processing | Gene expression in the silenced cells was compared with controls using AffylmGUI software, from www.bioconductor.org
| Sample_platform_id | GPL570
| Sample_contact_name | Giulia,,Calenda
| Sample_contact_email | giulia.calenda@einstein.yu.edu
| Sample_contact_department | Urology
| Sample_contact_institute | Albert Einstein College of Medicine
| Sample_contact_address | 1300 Morris Park Avenue
| Sample_contact_city | Bronx
| Sample_contact_state | NY
| Sample_contact_zip/postal_code | 10461
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM491nnn/GSM491174/suppl/GSM491174_KD1-HG-U133_Plus_2-3521.CEL.gz
| Sample_series_id | GSE19672
| Sample_data_row_count | 54675
| |
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