Search results for the GEO ID: GSE28503 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM706155 | GPL570 |
|
Control-SiMT
|
MCF-7 cell line transfected with non-targeting knockdown control psuper vector
|
cell line: MCF-7 breast cancer cell line
cell line source: 69 year old female
genotype/variation: control
|
Expression data from MCF-7 cell line transfected with non-targeting knockdown control psuper vector
|
Sample_geo_accession | GSM706155
| Sample_status | Public on Jul 01 2011
| Sample_submission_date | Apr 08 2011
| Sample_last_update_date | Jul 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | MCF-7 cell line was subjected to siRNA knockdown of either non-targeting, POLRMT, or PolII for 72 hours
| Sample_growth_protocol_ch1 | Cells were grown to 85 % confluence in 10 cm tissue culture dish.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each 10 cm dish was washed with 1x PBS for three times. Total RNA was extracted according to the RNeasy® Mini Kit Spin Protocol (QIAGEN). The integrity of the RNA extract was checked by 1.2 % (w/v) agarose gel electrophoresis and the concentration of RNA was estimated by ultraviolet spectrophotometry.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_hyb_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_scan_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_data_processing | MAS5.0 calculated signal intensities. Using scaling factor. The default settings are "scaling all probe sets to target signal: 500" and "normalization by user defined in value: 1
| Sample_platform_id | GPL570
| Sample_contact_name | Ming-Ta,,Hsu
| Sample_contact_email | kentkenpony@hotmail.com
| Sample_contact_institute | National Yang Ming University
| Sample_contact_address | No.155, Sec.2, Linong Street
| Sample_contact_city | Taipei
| Sample_contact_zip/postal_code | 112
| Sample_contact_country | Taiwan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706155/suppl/GSM706155.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706155/suppl/GSM706155.CHP.gz
| Sample_series_id | GSE28503
| Sample_series_id | GSE30350
| Sample_data_row_count | 54675
| |
|
GSM706156 | GPL570 |
|
SiMT-MCF-7
|
MCF-7 cell line transfected with targeting POLRMT psuper vector
|
cell line: MCF-7 breast cancer cell line
cell line source: 69 year old female
genotype/variation: POLRMT knockdown
|
Expression data from MCF-7 cell line transfected with targeting POLRMT psuper vector
|
Sample_geo_accession | GSM706156
| Sample_status | Public on Jul 01 2011
| Sample_submission_date | Apr 08 2011
| Sample_last_update_date | Jul 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | MCF-7 cell line was subjected to siRNA knockdown of either non-targeting, POLRMT, or PolII for 72 hours
| Sample_growth_protocol_ch1 | Cells were grown to 85 % confluence in 10 cm tissue culture dish.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each 10 cm dish was washed with 1x PBS for three times. Total RNA was extracted according to the RNeasy® Mini Kit Spin Protocol (QIAGEN). The integrity of the RNA extract was checked by 1.2 % (w/v) agarose gel electrophoresis and the concentration of RNA was estimated by ultraviolet spectrophotometry.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_hyb_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_scan_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_data_processing | MAS5.0 calculated signal intensities. Using scaling factor. The default settings are "scaling all probe sets to target signal: 500" and "normalization by user defined in value: 1
| Sample_platform_id | GPL570
| Sample_contact_name | Ming-Ta,,Hsu
| Sample_contact_email | kentkenpony@hotmail.com
| Sample_contact_institute | National Yang Ming University
| Sample_contact_address | No.155, Sec.2, Linong Street
| Sample_contact_city | Taipei
| Sample_contact_zip/postal_code | 112
| Sample_contact_country | Taiwan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706156/suppl/GSM706156.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706156/suppl/GSM706156.CHP.gz
| Sample_series_id | GSE28503
| Sample_series_id | GSE30350
| Sample_data_row_count | 54675
| |
|
GSM706157 | GPL570 |
|
Control-SiPolII
|
MCF-7 cell line transfected with non-targeting knockdown control psuper vector
|
cell line: MCF-7 breast cancer cell line
cell line source: 69 year old female
genotype/variation: control
|
Expression data from MCF-7 cell line transfected with non-targeting knockdown control psuper vector
|
Sample_geo_accession | GSM706157
| Sample_status | Public on Jul 01 2011
| Sample_submission_date | Apr 08 2011
| Sample_last_update_date | Jul 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | MCF-7 cell line was subjected to siRNA knockdown of either non-targeting, POLRMT, or PolII for 72 hours
| Sample_growth_protocol_ch1 | Cells were grown to 85 % confluence in 10 cm tissue culture dish.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each 10 cm dish was washed with 1x PBS for three times. Total RNA was extracted according to the RNeasy® Mini Kit Spin Protocol (QIAGEN). The integrity of the RNA extract was checked by 1.2 % (w/v) agarose gel electrophoresis and the concentration of RNA was estimated by ultraviolet spectrophotometry.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_hyb_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_scan_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_data_processing | MAS5.0 calculated signal intensities. Using scaling factor. The default settings are "scaling all probe sets to target signal: 500" and "normalization by user defined in value: 1
| Sample_platform_id | GPL570
| Sample_contact_name | Ming-Ta,,Hsu
| Sample_contact_email | kentkenpony@hotmail.com
| Sample_contact_institute | National Yang Ming University
| Sample_contact_address | No.155, Sec.2, Linong Street
| Sample_contact_city | Taipei
| Sample_contact_zip/postal_code | 112
| Sample_contact_country | Taiwan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706157/suppl/GSM706157.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706157/suppl/GSM706157.CHP.gz
| Sample_series_id | GSE28503
| Sample_series_id | GSE30350
| Sample_data_row_count | 54675
| |
|
GSM706158 | GPL570 |
|
SiPolII-MCF-7
|
MCF-7 cell line transfected with targeting PolII psuper vector
|
cell line: MCF-7 breast cancer cell line
cell line source: 69 year old female
genotype/variation: PolII knockdown
|
Expression data from MCF-7 cell line transfected with targeting PolII psuper vector
|
Sample_geo_accession | GSM706158
| Sample_status | Public on Jul 01 2011
| Sample_submission_date | Apr 08 2011
| Sample_last_update_date | Jul 01 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | MCF-7 cell line was subjected to siRNA knockdown of either non-targeting, POLRMT, or PolII for 72 hours
| Sample_growth_protocol_ch1 | Cells were grown to 85 % confluence in 10 cm tissue culture dish.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each 10 cm dish was washed with 1x PBS for three times. Total RNA was extracted according to the RNeasy® Mini Kit Spin Protocol (QIAGEN). The integrity of the RNA extract was checked by 1.2 % (w/v) agarose gel electrophoresis and the concentration of RNA was estimated by ultraviolet spectrophotometry.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_hyb_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_scan_protocol | Affymetrix microarray was performed using Human U133 2.0 (Affymetrix). Details of the methods for RNA quality, sample labeling, hybridization and expression analysis are according to the manual of Affymetrix Microarray Kit and Affymetrix website.
| Sample_data_processing | MAS5.0 calculated signal intensities. Using scaling factor. The default settings are "scaling all probe sets to target signal: 500" and "normalization by user defined in value: 1
| Sample_platform_id | GPL570
| Sample_contact_name | Ming-Ta,,Hsu
| Sample_contact_email | kentkenpony@hotmail.com
| Sample_contact_institute | National Yang Ming University
| Sample_contact_address | No.155, Sec.2, Linong Street
| Sample_contact_city | Taipei
| Sample_contact_zip/postal_code | 112
| Sample_contact_country | Taiwan
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706158/suppl/GSM706158.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM706nnn/GSM706158/suppl/GSM706158.CHP.gz
| Sample_series_id | GSE28503
| Sample_series_id | GSE30350
| Sample_data_row_count | 54675
| |
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