Search results for the GEO ID: GSE11133 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM280797 | GPL1355 |
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Ovary cultured control rep1
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4-day rat ovary cultured 2 days
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ovaries dissected from 4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
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mRNA from 4-day old rat ovaries cultured two days as controls with no treatment.
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Sample_geo_accession | GSM280797
| Sample_status | Public on Apr 11 2008
| Sample_submission_date | Apr 10 2008
| Sample_last_update_date | Apr 10 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Ovaries dissected from four-day old female rat pups were maintained in a whole organ culture system on floating filters (0.4 um Millicell-CM; Millipore Corp., Billerica, MA) in 0.5 ml DMEM-Ham’s F-12 medium (1:1, vol/vol; Life Technologies, Inc., Rockville, Maryland) containing 0.1% BSA (Sigma, St. Louis, MO), 0.1% albumax (Life Technologies, Inc., Rockville, Maryland), 200 ng/ml insulin (rh Insulin; Sigma, St. Louis, 10 MO), 0.05 mg/ml L-ascorbic acid (Sigma, St. Louis, MO) and 27.5 ug/ml transferrin (Sigma, St. Louis, MO) in a four-well culture plate (Nunc plate; Applied Scientific, South San Francisco, CA). Medium was supplemented with final concentration 5 ug/ml gentamicin, 3.25 ug/ml streptomycin, and 3.25 units/ml penicillin to prevent bacterial contamination. Ovaries were treated with no factor (control). Each sample contained 6-10 pooled ovaries, and no two ovaries from the same animal were placed into the same group.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | standard Affymetrix procedure
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using MAS5 preprocessing and a scaling factor of 125.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM280nnn/GSM280797/suppl/GSM280797.CEL.gz
| Sample_series_id | GSE11133
| Sample_data_row_count | 31099
| |
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GSM280798 | GPL1355 |
|
Ovary cultured control rep2
|
4-day rat ovary cultured 2 days
|
ovaries dissected from 4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
mRNA from 4-day old rat ovaries cultured two days as controls with no treatment.
|
Sample_geo_accession | GSM280798
| Sample_status | Public on Apr 11 2008
| Sample_submission_date | Apr 10 2008
| Sample_last_update_date | Apr 10 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Ovaries dissected from four-day old female rat pups were maintained in a whole organ culture system on floating filters (0.4 um Millicell-CM; Millipore Corp., Billerica, MA) in 0.5 ml DMEM-Ham’s F-12 medium (1:1, vol/vol; Life Technologies, Inc., Rockville, Maryland) containing 0.1% BSA (Sigma, St. Louis, MO), 0.1% albumax (Life Technologies, Inc., Rockville, Maryland), 200 ng/ml insulin (rh Insulin; Sigma, St. Louis, 10 MO), 0.05 mg/ml L-ascorbic acid (Sigma, St. Louis, MO) and 27.5 ug/ml transferrin (Sigma, St. Louis, MO) in a four-well culture plate (Nunc plate; Applied Scientific, South San Francisco, CA). Medium was supplemented with final concentration 5 ug/ml gentamicin, 3.25 ug/ml streptomycin, and 3.25 units/ml penicillin to prevent bacterial contamination. Ovaries were treated with no factor (control). Each sample contained 6-10 pooled ovaries, and no two ovaries from the same animal were placed into the same group.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | standard Affymetrix procedure
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using MAS5 preprocessing and a scaling factor of 125.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM280nnn/GSM280798/suppl/GSM280798.CEL.gz
| Sample_series_id | GSE11133
| Sample_data_row_count | 31099
| |
|
GSM280799 | GPL1355 |
|
Ovary cultured GDNF rep1
|
4-day rat ovary cultured 2 days
|
ovaries dissected from 4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
mRNA from 4-day old rat ovaries cultured two days with GDNF treatment.
|
Sample_geo_accession | GSM280799
| Sample_status | Public on Apr 11 2008
| Sample_submission_date | Apr 10 2008
| Sample_last_update_date | Apr 10 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Ovaries dissected from four-day old female rat pups were maintained in a whole organ culture system on floating filters (0.4 um Millicell-CM; Millipore Corp., Billerica, MA) in 0.5 ml DMEM-Ham’s F-12 medium (1:1, vol/vol; Life Technologies, Inc., Rockville, Maryland) containing 0.1% BSA (Sigma, St. Louis, MO), 0.1% albumax (Life Technologies, Inc., Rockville, Maryland), 200 ng/ml insulin (rh Insulin; Sigma, St. Louis, 10 MO), 0.05 mg/ml L-ascorbic acid (Sigma, St. Louis, MO) and 27.5 ug/ml transferrin (Sigma, St. Louis, MO) in a four-well culture plate (Nunc plate; Applied Scientific, South San Francisco, CA). Medium was supplemented with final concentration 5 ug/ml gentamicin, 3.25 ug/ml streptomycin, and 3.25 units/ml penicillin to prevent bacterial contamination. Ovaries were treated with no factor (control). Each sample contained 6-10 pooled ovaries, and no two ovaries from the same animal were placed into the same group.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | standard Affymetrix procedure
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using MAS5 preprocessing and a scaling factor of 125.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM280nnn/GSM280799/suppl/GSM280799.CEL.gz
| Sample_series_id | GSE11133
| Sample_data_row_count | 31099
| |
|
GSM280800 | GPL1355 |
|
Ovary cultured GDNF rep2
|
4-day rat ovary cultured 2 days
|
ovaries dissected from 4-day old Sprague-Dawley rats and cleaned of ovarian bursa.
|
mRNA from 4-day old rat ovaries cultured two days with GDNF treatment.
|
Sample_geo_accession | GSM280800
| Sample_status | Public on Apr 11 2008
| Sample_submission_date | Apr 10 2008
| Sample_last_update_date | Apr 10 2008
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Ovaries dissected from four-day old female rat pups were maintained in a whole organ culture system on floating filters (0.4 um Millicell-CM; Millipore Corp., Billerica, MA) in 0.5 ml DMEM-Ham’s F-12 medium (1:1, vol/vol; Life Technologies, Inc., Rockville, Maryland) containing 0.1% BSA (Sigma, St. Louis, MO), 0.1% albumax (Life Technologies, Inc., Rockville, Maryland), 200 ng/ml insulin (rh Insulin; Sigma, St. Louis, 10 MO), 0.05 mg/ml L-ascorbic acid (Sigma, St. Louis, MO) and 27.5 ug/ml transferrin (Sigma, St. Louis, MO) in a four-well culture plate (Nunc plate; Applied Scientific, South San Francisco, CA). Medium was supplemented with final concentration 5 ug/ml gentamicin, 3.25 ug/ml streptomycin, and 3.25 units/ml penicillin to prevent bacterial contamination. Ovaries were treated with no factor (control). Each sample contained 6-10 pooled ovaries, and no two ovaries from the same animal were placed into the same group.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Ovaries with the same treatment were pooled to make each RNA sample. RNA was extracted using the Trizol reagent according to manufacturers instructions (Sigma, St. Louis, MO).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | standard Affymetrix procedures
| Sample_hyb_protocol | standard Affymetrix procedure
| Sample_scan_protocol | standard Affymetrix procedure
| Sample_data_processing = Auto-scale ON (1-1000). Scaling | all probe sets. The microarray image data were converted to numerical data with GeneChip Operating Software using MAS5 preprocessing and a scaling factor of 125.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,K,Skinner
| Sample_contact_email | skinner@mail.wsu.edu
| Sample_contact_department | SBS
| Sample_contact_institute | WSU
| Sample_contact_address | Abelson 507
| Sample_contact_city | Pullman
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 99163
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM280nnn/GSM280800/suppl/GSM280800.CEL.gz
| Sample_series_id | GSE11133
| Sample_data_row_count | 31099
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