Home   Search   Browse   Statistics   User guide   FAQs   Post question   Download   Process data  
Search results for the GEO ID: GSE10479
(Click on the check boxes provided under "Select for analysis", to initiate grouping)
(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down)
GSM ID
GPL ID
Select for analysis
Title
Source name
Description
Characteristics
GSM265052
GPL570
bg-CAT treated HUVECs, biological rep1 primary cultured HUVECs treated with bg-CAT (25 nM, 2 h) Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from HUVECs treated with bg-CAT (25 nM) for 2 hour
GSM265053
GPL570
bg-CAT treated HUVECs, biological rep2 primary cultured HUVECs treated with bg-CAT (25 nM, 2 h) Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from HUVECs treated with bg-CAT (25 nM) for 2 hour
GSM265054
GPL570
bg-CAT treated HUVECs, biological rep3 primary cultured HUVECs treated with bg-CAT (25 nM, 2 h) Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from HUVECs treated with bg-CAT (25 nM) for 2 hour
GSM265055
GPL570
bg-CAT treated HUVECs, biological rep4 primary cultured HUVECs treated with bg-CAT (25 nM, 2 h) Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from HUVECs treated with bg-CAT (25 nM) for 2 hour
GSM265056
GPL570
HUVECs normal Control, biological rep1 primary cultured HUVECs treated with PBS as a normal control Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from normal control HUVECs
GSM265057
GPL570
HUVECs normal Control, biological rep2 primary cultured HUVECs treated with PBS as a normal control Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from normal control HUVECs
GSM265058
GPL570
HUVECs normal Control, biological rep3 primary cultured HUVECs treated with PBS as a normal control Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from normal control HUVECs
GSM265059
GPL570
HUVECs normal Control, biological rep4 primary cultured HUVECs treated with PBS as a normal control Primary cultured HUVECs used in the experiments were confluent monolayers between passages 2 and 3. The primary cultured HUVECs were confirmed by positive staining of indirect immunofluorescence with thrombomodulin (monoclonal antibody). Gene expression data from normal control HUVECs
 
 
Make groups for comparisons
(2 groups will be compared at a time)
Select GSMs and click on "Add groups"
Enter the group name here:


Select expression type
Transcripts profile based on;
A. Differential status (Up/Down regulation)
B. Absolute calls (Transcribed/Not-detected)
 
Filter results by number of probes