Search results for the GEO ID: GSE35755 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM874443 | GPL1261 |
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Control (hetzerozygous littermates)
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primary sertoli cells from 3 days old mice
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strain: C57BL/6
genotype/variation: control
age: 3 days old
cell type: primary sertoli cells
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Gene expression data from primary sertoli cells of 3 days old mice
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Sample_geo_accession | GSM874443
| Sample_status | Public on Feb 13 2012
| Sample_submission_date | Feb 13 2012
| Sample_last_update_date | Feb 14 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | 3 days old mice were anesthetized with CO2 and then killed by cervical dislocation. Decapsulated testes were incubated with 2 mg/ml collagena (Gibco, Invitrogen, Carlsbad, CA, USA) at room temperature for 10 min with gentle oscillation and then filtered through 80 um copper meshes to remove interstitial cells. The seminiferous tubules were resuspended in the collagenase at room temperature for an additional 15 min to remove myoid cells. The tubules were then incubated with 0.5 mg/ml hyaluronidase (Sigma, St. Louis, MO, USA) at room temperature for 15 min with gentle oscillation and pipetting. After washing twice with PBS, the cells were cultured in DMEM /F12 (Sigma, St. Louis, MO, USA) supplemented with sodium bicarbonate (1.2 mg/ml), penicillin (100 U/ml), streptomycin (100 mg/ml), and 10% fetal bovine serum (Life Technologies, Gaithersburg, MD, USA). The cells were maintained in a humidified atmosphere containing5% CO2 at 37 ℃ for 24 h. After the incubation, cells were treated with a hypotonic solution (20 mM Tris, pH 7.4) for 1 min to remove the spermatogenic cells adhering to the Sertoli cells.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After cultured sertoli cell twenty-four hours, cell were washed with PBS and placed on ice in the Trizol solution (invitrogen,Carlsbad, CA, USA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 500ng total RNA (3_ivt_express_kit_manual Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix Scanner 7G.
| Sample_data_processing | The data were analyzed with PARTEK genomic suit 6.4 using RMA normalization
| Sample_platform_id | GPL1261
| Sample_contact_name | Xiu-Xing,,Wang
| Sample_contact_email | xiuxing81@yahoo.com.cn
| Sample_contact_phone | 862583596289
| Sample_contact_fax | 862583596289
| Sample_contact_department | MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center and the School of Medicine
| Sample_contact_institute | Nanjing University
| Sample_contact_address | #22 Hankou Road
| Sample_contact_city | Nanjing
| Sample_contact_state | Jiangsu
| Sample_contact_zip/postal_code | 210093
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM874nnn/GSM874443/suppl/GSM874443.CEL.gz
| Sample_series_id | GSE35755
| Sample_data_row_count | 45101
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GSM874444 | GPL1261 |
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KO
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primary sertoli cells from 3 days old mice
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strain: C57BL/6
genotype/variation: GGPP knockout
age: 3 days old
cell type: primary sertoli cells
|
Gene expression data from primary sertoli cells of 3 days old mice
|
Sample_geo_accession | GSM874444
| Sample_status | Public on Feb 13 2012
| Sample_submission_date | Feb 13 2012
| Sample_last_update_date | Feb 14 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | 3 days old mice were anesthetized with CO2 and then killed by cervical dislocation. Decapsulated testes were incubated with 2 mg/ml collagena (Gibco, Invitrogen, Carlsbad, CA, USA) at room temperature for 10 min with gentle oscillation and then filtered through 80 um copper meshes to remove interstitial cells. The seminiferous tubules were resuspended in the collagenase at room temperature for an additional 15 min to remove myoid cells. The tubules were then incubated with 0.5 mg/ml hyaluronidase (Sigma, St. Louis, MO, USA) at room temperature for 15 min with gentle oscillation and pipetting. After washing twice with PBS, the cells were cultured in DMEM /F12 (Sigma, St. Louis, MO, USA) supplemented with sodium bicarbonate (1.2 mg/ml), penicillin (100 U/ml), streptomycin (100 mg/ml), and 10% fetal bovine serum (Life Technologies, Gaithersburg, MD, USA). The cells were maintained in a humidified atmosphere containing5% CO2 at 37 ℃ for 24 h. After the incubation, cells were treated with a hypotonic solution (20 mM Tris, pH 7.4) for 1 min to remove the spermatogenic cells adhering to the Sertoli cells.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After cultured sertoli cell twenty-four hours, cell were washed with PBS and placed on ice in the Trizol solution (invitrogen,Carlsbad, CA, USA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 500ng total RNA (3_ivt_express_kit_manual Affymetrix).
| Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix Scanner 7G.
| Sample_data_processing | The data were analyzed with PARTEK genomic suit 6.4 using RMA normalization
| Sample_platform_id | GPL1261
| Sample_contact_name | Xiu-Xing,,Wang
| Sample_contact_email | xiuxing81@yahoo.com.cn
| Sample_contact_phone | 862583596289
| Sample_contact_fax | 862583596289
| Sample_contact_department | MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center and the School of Medicine
| Sample_contact_institute | Nanjing University
| Sample_contact_address | #22 Hankou Road
| Sample_contact_city | Nanjing
| Sample_contact_state | Jiangsu
| Sample_contact_zip/postal_code | 210093
| Sample_contact_country | China
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM874nnn/GSM874444/suppl/GSM874444.CEL.gz
| Sample_series_id | GSE35755
| Sample_data_row_count | 45101
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