Search results for the GEO ID: GSE1776 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM30759 | GPL339 |
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CON_A
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C2C12 MYOTUBES
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CONTROL MYOTUBES
C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
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Sample_geo_accession | GSM30759
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30759/suppl/GSM30759.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30771 | GPL339 |
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CON_B
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C2C12 MYTOUBES
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CONTROL MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30771
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30771/suppl/GSM30771.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30772 | GPL339 |
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CON_C
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C2C12 MYOTUBES
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CONTROL MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30772
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30772/suppl/GSM30772.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30773 | GPL339 |
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CON_D
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C2C12 MYOTUBES
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CONTROL MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30773
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30773/suppl/GSM30773.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30774 | GPL339 |
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STV_E
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C2C12 MYOTUBES STARVED 4 DAYS
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STARVED MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30774
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30774/suppl/GSM30774.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30775 | GPL339 |
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STV_F
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C2C12 MYOTUBES STARVED 4 DAYS
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|
STARVED MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30775
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30775/suppl/GSM30775.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
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GSM30776 | GPL339 |
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STV_G
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C2C12 MYOTUBES STARVED 4 DAYS
|
|
STARVED MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30776
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30776/suppl/GSM30776.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
| |
|
GSM30777 | GPL339 |
|
STV_H
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C2C12 MYOTUBES STARVED 4 DAYS
|
|
STARVED MYOTUBES - C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and "starved" (non re-fed cells)
Keywords = skeletal muscle
Keywords = atrophy
|
Sample_geo_accession | GSM30777
| Sample_status | Public on Sep 20 2004
| Sample_submission_date | Sep 17 2004
| Sample_last_update_date | May 27 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_molecule_ch1 | total RNA
| Sample_platform_id | GPL339
| Sample_contact_name | Susan,,Kandarian
| Sample_contact_email | skandar@bu.edu
| Sample_contact_phone | 617-353-7493
| Sample_contact_department | Department of Health Sciences
| Sample_contact_institute | Boston University
| Sample_contact_address |
| Sample_contact_city | Boston
| Sample_contact_state | MA
| Sample_contact_zip/postal_code | 02215
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM30nnn/GSM30777/suppl/GSM30777.CEL.gz
| Sample_series_id | GSE1776
| Sample_data_row_count | 22690
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